Canonical Allele Identifier: CA1190285878
Gene: NRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114707399T= , CM000663.2:g.114707399T= GRCh38
NC_000001.10:g.115250020T= , CM000663.1:g.115250020T= GRCh37
NC_000001.9:g.115051543T= NCBI36
NG_007572.1:g.14496A= , LRG_92:g.14496A=

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*695A= MANE Select ENSP00000358548.4:n.*695A=
ENST00000369535.4:c.*695A= ENSP00000358548.4:n.*695A=
NM_002524.4:c.*695A= NP_002515.1:n.*695A=
NM_002524.5:c.*695A= MANE Select NP_002515.1:n.*695A=
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