Canonical Allele Identifier: CA1190292150
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114716023G= , CM000663.2:g.114716023G= GRCh38
NC_000001.10:g.115258644G= , CM000663.1:g.115258644G= GRCh37
NC_000001.9:g.115060167G= NCBI36
NG_007572.1:g.5872C= , LRG_92:g.5872C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.111+27C= MANE Select ENSP00000358548.4:n.111+27C=
ENST00000369535.4:c.111+27C= ENSP00000358548.4:n.111+27C=
NM_002524.4:c.111+27C= NP_002515.1:n.111+27C=
NM_002524.5:c.111+27C= MANE Select NP_002515.1:n.111+27C=