Canonical Allele Identifier: CA1148021343
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709850G= , CM000663.2:g.114709850G= GRCh38
NC_000001.10:g.115252471G= , CM000663.1:g.115252471G= GRCh37
NC_000001.9:g.115053994G= NCBI36
NG_007572.1:g.12045C= , LRG_92:g.12045C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.291-122C= MANE Select ENSP00000358548.4:n.291-122C=
ENST00000369535.4:c.291-122C= ENSP00000358548.4:n.291-122C=
NM_002524.4:c.291-122C= NP_002515.1:n.291-122C=
NM_002524.5:c.291-122C= MANE Select NP_002515.1:n.291-122C=