Canonical Allele Identifier: CA1190284771
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705853T= , CM000663.2:g.114705853T= GRCh38
NC_000001.10:g.115248474T= , CM000663.1:g.115248474T= GRCh37
NC_000001.9:g.115049997T= NCBI36
NG_007572.1:g.16042A= , LRG_92:g.16042A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*2241A= MANE Select ENSP00000358548.4:n.*2241A=
ENST00000369535.4:c.*2241A= ENSP00000358548.4:n.*2241A=
NM_002524.4:c.*2241A= NP_002515.1:n.*2241A=
NM_002524.5:c.*2241A= MANE Select NP_002515.1:n.*2241A=