Canonical Allele Identifier: CA1141580983
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713907T= , CM000663.2:g.114713907T= GRCh38
NC_000001.10:g.115256528T= , CM000663.1:g.115256528T= GRCh37
NC_000001.9:g.115058051T= NCBI36
NG_007572.1:g.7988A= , LRG_92:g.7988A=

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.183A= MANE Select ENSP00000358548.4:p.Gln61=
ENST00000369535.4:c.183A= ENSP00000358548.4:p.Gln61=
NM_002524.4:c.183A= NP_002515.1:p.Gln61=
NM_002524.5:c.183A= MANE Select NP_002515.1:p.Gln61=