Canonical Allele Identifier: CA1190291283
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713807G= , CM000663.2:g.114713807G= GRCh38
NC_000001.10:g.115256428G= , CM000663.1:g.115256428G= GRCh37
NC_000001.9:g.115057951G= NCBI36
NG_007572.1:g.8088C= , LRG_92:g.8088C=

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.283C= MANE Select ENSP00000358548.4:p.Leu95=
ENST00000369535.4:c.283C= ENSP00000358548.4:p.Leu95=
NM_002524.4:c.283C= NP_002515.1:p.Leu95=
NM_002524.5:c.283C= MANE Select NP_002515.1:p.Leu95=