Canonical Allele Identifier: CA645537989
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101742018
COSMIC: COSM53223

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713907_114713909delinsCTT , CM000663.2:g.114713907_114713909delinsCTT GRCh38
NC_000001.10:g.115256528_115256530delinsCTT , CM000663.1:g.115256528_115256530delinsCTT GRCh37
NC_000001.9:g.115058051_115058053delinsCTT NCBI36
NG_007572.1:g.7986_7988delinsAAG , LRG_92:g.7986_7988delinsAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.181_183delinsAAG MANE Select ENSP00000358548.4:p.Gln61Lys
ENST00000369535.4:c.181_183delinsAAG ENSP00000358548.4:p.Gln61Lys
NM_002524.4:c.181_183delinsAAG NP_002515.1:p.Gln61Lys
NM_002524.5:c.181_183delinsAAG MANE Select NP_002515.1:p.Gln61Lys