Canonical Allele Identifier: CA2647250255
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114706010dup , CM000663.2:g.114706010dup GRCh38
NC_000001.10:g.115248631dup , CM000663.1:g.115248631dup GRCh37
NC_000001.9:g.115050154dup NCBI36
NG_007572.1:g.15885dup , LRG_92:g.15885dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*2084dup MANE Select ENSP00000358548.4:n.*2084dup
ENST00000369535.4:c.*2084dup ENSP00000358548.4:n.*2084dup
NM_002524.4:c.*2084dup NP_002515.1:n.*2084dup
NM_002524.5:c.*2084dup MANE Select NP_002515.1:n.*2084dup