Canonical Allele Identifier: CA341739203
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1433700836

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709609T>A , CM000663.2:g.114709609T>A GRCh38
NC_000001.10:g.115252230T>A , CM000663.1:g.115252230T>A GRCh37
NC_000001.9:g.115053753T>A NCBI36
NG_007572.1:g.12286A>T , LRG_92:g.12286A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.410A>T MANE Select ENSP00000358548.4:p.Tyr137Phe
ENST00000369535.4:c.410A>T ENSP00000358548.4:p.Tyr137Phe
NM_002524.4:c.410A>T NP_002515.1:p.Tyr137Phe
NM_002524.5:c.410A>T MANE Select NP_002515.1:p.Tyr137Phe