Canonical Allele Identifier: CA1190291285
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713813T= , CM000663.2:g.114713813T= GRCh38
NC_000001.10:g.115256434T= , CM000663.1:g.115256434T= GRCh37
NC_000001.9:g.115057957T= NCBI36
NG_007572.1:g.8082A= , LRG_92:g.8082A=

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.277A= MANE Select ENSP00000358548.4:p.Ile93=
ENST00000369535.4:c.277A= ENSP00000358548.4:p.Ile93=
NM_002524.4:c.277A= NP_002515.1:p.Ile93=
NM_002524.5:c.277A= MANE Select NP_002515.1:p.Ile93=