Canonical Allele Identifier: CA1145302026
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709930T= , CM000663.2:g.114709930T= GRCh38
NC_000001.10:g.115252551T= , CM000663.1:g.115252551T= GRCh37
NC_000001.9:g.115054074T= NCBI36
NG_007572.1:g.11965A= , LRG_92:g.11965A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.291-202A= MANE Select ENSP00000358548.4:n.291-202A=
ENST00000369535.4:c.291-202A= ENSP00000358548.4:n.291-202A=
NM_002524.4:c.291-202A= NP_002515.1:n.291-202A=
NM_002524.5:c.291-202A= MANE Select NP_002515.1:n.291-202A=