ClinVar

NM_005343.4(HRAS):c.37G>T (p.Gly13Cys)

Genes:

HRAS:HRas proto-oncogene, GTPase [Gene - OMIM - HGNC]
LRRC56:leucine rich repeat containing 56 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11p15.5

Genomic location:

• Chr11: 534286 (on Assembly GRCh38)
• Chr11: 534286 (on Assembly GRCh37)

Preferred name:

NM_005343.4(HRAS):c.37G>T (p.Gly13Cys)

Other names:

p.G13C:GGT>TGT; NM_005343.3(HRAS):c.37G>T

HGVS:

• NC_000011.10:g.534286C>A
• NG_007666.1:g.6265G>T
• NM_001130442.3:c.37G>T
• NM_001318054.2:c.-283G>T
• NM_005343.4:c.37G>TMANE SELECT
• NM_176795.5:c.37G>T
• NP_001123914.1:p.Gly13Cys
• NP_005334.1:p.Gly13Cys
• NP_789765.1:p.Gly13Cys
• LRG_506t1:c.37G>T
• LRG_506:g.6265G>T
• LRG_506p1:p.Gly13Cys
• NC_000011.9:g.534286C>A
• NM_005343.2:c.37G>T
• NM_005343.3:c.37G>T
• P01112:p.Gly13Cys
• c.37G>T

This HGVS expression did not pass validation

Protein change:

G13C; GLY13CYS

Links:

UniProtKB: P01112#VAR_026107; OMIM: 190020.0007; dbSNP: rs104894228

NCBI 1000 Genomes Browser:

rs104894228

Molecular consequence:

• NM_001318054.2:c.-283G>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001130442.3:c.37G>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_005343.4:c.37G>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_176795.5:c.37G>T - missense variant - [Sequence Ontology: SO:0001583]