Canonical Allele Identifier: CA441393036

Gene: NAA15

Linked Data

• MyVariant Identifiers: chr4:g.140258078T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336924T>G , CM000666.2:g.139336924T>G	GRCh38
NC_000004.11:g.140258078T>G , CM000666.1:g.140258078T>G	GRCh37
NC_000004.10:g.140477528T>G	NCBI36
NG_053037.1:g.40458T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.216T>G	ENSP00000514912.1:p.Gly72=
ENST00000700275.1:c.216T>G	ENSP00000514910.1:p.Gly72=
ENST00000700276.1:c.139+2666T>G	ENSP00000514911.1:n.139+2666T>G
ENST00000700277.1:c.216T>G	ENSP00000514913.1:p.Gly72=
ENST00000700278.1:n.393T>G
ENST00000700279.1:n.474T>G
ENST00000296543.10:c.216T>G MANE Select	ENSP00000296543.4:p.Gly72=
ENST00000296543.9:c.216T>G	ENSP00000296543.4:p.Gly72=
ENST00000398947.1:c.216T>G	ENSP00000381920.1:p.Gly72=
ENST00000480277.2:n.52T>G
ENST00000482087.1:n.360T>G
NM_057175.3:c.216T>G	NP_476516.1:p.Gly72=
XM_005263236.1:c.216T>G	XP_005263293.1:p.Gly72=
NM_057175.4:c.216T>G	NP_476516.1:p.Gly72=
XM_005263236.3:c.216T>G	XP_005263293.1:p.Gly72=
NM_057175.5:c.216T>G MANE Select	NP_476516.1:p.Gly72=