Canonical Allele Identifier: CA1148224479
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713915C= , CM000663.2:g.114713915C= GRCh38
NC_000001.10:g.115256536C= , CM000663.1:g.115256536C= GRCh37
NC_000001.9:g.115058059C= NCBI36
NG_007572.1:g.7980G= , LRG_92:g.7980G=

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.175G= MANE Select ENSP00000358548.4:p.Ala59=
ENST00000369535.4:c.175G= ENSP00000358548.4:p.Ala59=
NM_002524.4:c.175G= NP_002515.1:p.Ala59=
NM_002524.5:c.175G= MANE Select NP_002515.1:p.Ala59=