Canonical Allele Identifier: CA441392872

Gene: NAA15

Linked Data

• gnomAD v4: 4-139336897-A-G
• MyVariant Identifiers: chr4:g.140258051A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336897A>G , CM000666.2:g.139336897A>G	GRCh38
NC_000004.11:g.140258051A>G , CM000666.1:g.140258051A>G	GRCh37
NC_000004.10:g.140477501A>G	NCBI36
NG_053037.1:g.40431A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.189A>G	ENSP00000514912.1:p.Glu63=
ENST00000700275.1:c.189A>G	ENSP00000514910.1:p.Glu63=
ENST00000700276.1:c.139+2639A>G	ENSP00000514911.1:n.139+2639A>G
ENST00000700277.1:c.189A>G	ENSP00000514913.1:p.Glu63=
ENST00000700278.1:n.366A>G
ENST00000700279.1:n.447A>G
ENST00000296543.10:c.189A>G MANE Select	ENSP00000296543.4:p.Glu63=
ENST00000296543.9:c.189A>G	ENSP00000296543.4:p.Glu63=
ENST00000398947.1:c.189A>G	ENSP00000381920.1:p.Glu63=
ENST00000480277.2:n.25A>G
ENST00000482087.1:n.333A>G
NM_057175.3:c.189A>G	NP_476516.1:p.Glu63=
XM_005263236.1:c.189A>G	XP_005263293.1:p.Glu63=
NM_057175.4:c.189A>G	NP_476516.1:p.Glu63=
XM_005263236.3:c.189A>G	XP_005263293.1:p.Glu63=
NM_057175.5:c.189A>G MANE Select	NP_476516.1:p.Glu63=