Canonical Allele Identifier: CA1143648811
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709776C= , CM000663.2:g.114709776C= GRCh38
NC_000001.10:g.115252397C= , CM000663.1:g.115252397C= GRCh37
NC_000001.9:g.115053920C= NCBI36
NG_007572.1:g.12119G= , LRG_92:g.12119G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.291-48G= MANE Select ENSP00000358548.4:n.291-48G=
ENST00000369535.4:c.291-48G= ENSP00000358548.4:n.291-48G=
NM_002524.4:c.291-48G= NP_002515.1:n.291-48G=
NM_002524.5:c.291-48G= MANE Select NP_002515.1:n.291-48G=