Canonical Allele Identifier: CA645537992
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1057519834
COSMIC: COSM12725

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713908_114713909delinsAA , CM000663.2:g.114713908_114713909delinsAA GRCh38
NC_000001.10:g.115256529_115256530delinsAA , CM000663.1:g.115256529_115256530delinsAA GRCh37
NC_000001.9:g.115058052_115058053delinsAA NCBI36
NG_007572.1:g.7986_7987delinsTT , LRG_92:g.7986_7987delinsTT

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.181_182delinsTT MANE Select ENSP00000358548.4:p.Gln61Leu
ENST00000369535.4:c.181_182delinsTT ENSP00000358548.4:p.Gln61Leu
NM_002524.4:c.181_182delinsTT NP_002515.1:p.Gln61Leu
NM_002524.5:c.181_182delinsTT MANE Select NP_002515.1:p.Gln61Leu