Canonical Allele Identifier: CA1498317693

Gene: NAA15

Linked Data

• dbSNP Id: rs1747211453

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336670C>A , CM000666.2:g.139336670C>A	GRCh38
NC_000004.11:g.140257824C>A , CM000666.1:g.140257824C>A	GRCh37
NC_000004.10:g.140477274C>A	NCBI36
NG_053037.1:g.40204C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.140-178C>A	ENSP00000514912.1:n.140-178C>A
ENST00000700275.1:c.140-178C>A	ENSP00000514910.1:n.140-178C>A
ENST00000700276.1:c.139+2412C>A	ENSP00000514911.1:n.139+2412C>A
ENST00000700277.1:c.140-178C>A	ENSP00000514913.1:n.140-178C>A
ENST00000700278.1:n.317-178C>A
ENST00000700279.1:n.398-178C>A
ENST00000296543.10:c.140-178C>A MANE Select	ENSP00000296543.4:n.140-178C>A
ENST00000296543.9:c.140-178C>A	ENSP00000296543.4:n.140-178C>A
ENST00000398947.1:c.140-178C>A	ENSP00000381920.1:n.140-178C>A
ENST00000482087.1:n.284-178C>A
NM_057175.3:c.140-178C>A	NP_476516.1:n.140-178C>A
XM_005263236.1:c.140-178C>A	XP_005263293.1:n.140-178C>A
NM_057175.4:c.140-178C>A	NP_476516.1:n.140-178C>A
XM_005263236.3:c.140-178C>A	XP_005263293.1:n.140-178C>A
NM_057175.5:c.140-178C>A MANE Select	NP_476516.1:n.140-178C>A