Canonical Allele Identifier: CA290041598

Gene: TAF15

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35844834G>A , CM000679.2:g.35844834G>A	GRCh38
NC_000017.9:g.31195951G>A	NCBI36
NG_023279.1:g.40351G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_139215.3:c.1535G>A MANE Select	NP_631961.1:p.Arg512Gln
ENST00000605844.6:c.1535G>A MANE Select	ENSP00000474096.1:p.Arg512Gln
NM_003487.3:c.1526G>A	NP_003478.1:p.Arg509Gln
NM_003487.4:c.1526G>A	NP_003478.1:p.Arg509Gln
NM_139215.2:c.1535G>A	NP_631961.1:p.Arg512Gln
ENST00000603067.6:n.4015G>A
ENST00000603777.5:c.995-46G>A	ENSP00000474522.1:n.995-46G>A
ENST00000603777.6:c.*1033G>A	ENSP00000474522.2:n.*1033G>A
ENST00000604694.1:c.424-24G>A
ENST00000604694.2:c.*861G>A	ENSP00000475147.2:n.*861G>A
ENST00000604841.5:c.1526G>A	ENSP00000474609.1:p.Arg509Gln
ENST00000605844.5:c.1535G>A	ENSP00000474096.1:p.Arg512Gln
ENST00000687618.1:n.1021G>A
ENST00000689923.1:n.1792G>A
XM_011525314.1:c.1451G>A	XP_011523616.1:p.Arg484Gln
XM_011525315.1:c.1262G>A	XP_011523617.1:p.Arg421Gln
XM_024450959.1:c.728G>A	XP_024306727.1:p.Arg243Gln