Canonical Allele Identifier: CA2647248627
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114714014_114714015insTT , CM000663.2:g.114714014_114714015insTT GRCh38
NC_000001.10:g.115256635_115256636insTT , CM000663.1:g.115256635_115256636insTT GRCh37
NC_000001.9:g.115058158_115058159insTT NCBI36
NG_007572.1:g.7880_7881insAA , LRG_92:g.7880_7881insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.112-37_112-36insAA MANE Select ENSP00000358548.4:n.112-37_112-36insAA
ENST00000369535.4:c.112-37_112-36insAA ENSP00000358548.4:n.112-37_112-36insAA
NM_002524.4:c.112-37_112-36insAA NP_002515.1:n.112-37_112-36insAA
NM_002524.5:c.112-37_112-36insAA MANE Select NP_002515.1:n.112-37_112-36insAA