Canonical Allele Identifier: CA2647249015
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114716032G>T , CM000663.2:g.114716032G>T GRCh38
NC_000001.10:g.115258653G>T , CM000663.1:g.115258653G>T GRCh37
NC_000001.9:g.115060176G>T NCBI36
NG_007572.1:g.5863C>A , LRG_92:g.5863C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.111+18C>A MANE Select ENSP00000358548.4:n.111+18C>A
ENST00000369535.4:c.111+18C>A ENSP00000358548.4:n.111+18C>A
NM_002524.4:c.111+18C>A NP_002515.1:n.111+18C>A
NM_002524.5:c.111+18C>A MANE Select NP_002515.1:n.111+18C>A