Canonical Allele Identifier: CA29045018

Gene: NRAS

Linked Data

• dbSNP Id: rs147650587

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114714008dup , CM000663.2:g.114714008dup	GRCh38
NC_000001.10:g.115256629dup , CM000663.1:g.115256629dup	GRCh37
NC_000001.9:g.115058152dup	NCBI36
NG_007572.1:g.7887dup , LRG_92:g.7887dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.112-30dup MANE Select	ENSP00000358548.4:n.112-30dup
ENST00000369535.4:c.112-30dup	ENSP00000358548.4:n.112-30dup
NM_002524.4:c.112-30dup	NP_002515.1:n.112-30dup
NM_002524.5:c.112-30dup MANE Select	NP_002515.1:n.112-30dup