Canonical Allele Identifier: CA358259793

Gene: NAA15

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139340994G>A , CM000666.2:g.139340994G>A	GRCh38
NC_000004.11:g.140262148G>A , CM000666.1:g.140262148G>A	GRCh37
NC_000004.10:g.140481598G>A	NCBI36
NG_053037.1:g.44528G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.327G>A	ENSP00000514912.1:p.Trp109Ter
ENST00000700275.1:c.327G>A	ENSP00000514910.1:p.Trp109Ter
ENST00000700276.1:c.140-1832G>A	ENSP00000514911.1:n.140-1832G>A
ENST00000700277.1:c.241-46G>A	ENSP00000514913.1:n.241-46G>A
ENST00000700278.1:n.504G>A
ENST00000700279.1:n.585G>A
ENST00000296543.10:c.327G>A MANE Select	ENSP00000296543.4:p.Trp109Ter
ENST00000296543.9:c.327G>A	ENSP00000296543.4:p.Trp109Ter
ENST00000398947.1:c.327G>A	ENSP00000381920.1:p.Trp109Ter
ENST00000480277.2:n.163G>A
ENST00000482087.1:n.471G>A
NM_057175.3:c.327G>A	NP_476516.1:p.Trp109Ter
XM_005263236.1:c.327G>A	XP_005263293.1:p.Trp109Ter
NM_057175.4:c.327G>A	NP_476516.1:p.Trp109Ter
XM_005263236.3:c.327G>A	XP_005263293.1:p.Trp109Ter
NM_057175.5:c.327G>A MANE Select	NP_476516.1:p.Trp109Ter