Canonical Allele Identifier: CA413537444

Gene: TAF1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71408062G>A , CM000685.2:g.71408062G>A	GRCh38
NC_000023.10:g.70627912G>A , CM000685.1:g.70627912G>A	GRCh37
NC_000023.9:g.70544637G>A	NCBI36
NG_012771.2:g.46799G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004606.5:c.4295G>A MANE Select	NP_004597.3:p.Arg1432His
ENST00000423759.6:c.4295G>A MANE Select	ENSP00000406549.2:p.Arg1432His
NM_001286074.1:c.4355G>A	NP_001273003.1:p.Arg1452His
NM_001286074.2:c.4295G>A	NP_001273003.2:p.Arg1432His
NM_004606.4:c.4355G>A	NP_004597.2:p.Arg1452His
NM_138923.3:c.4292G>A	NP_620278.1:p.Arg1431His
NM_138923.4:c.4232G>A	NP_620278.2:p.Arg1411His
NR_104387.1:n.4431G>A
NR_104387.2:n.4313G>A
NR_104388.1:n.4431G>A
NR_104388.2:n.4313G>A
NR_104389.1:n.4431G>A
NR_104389.2:n.4313G>A
NR_104390.1:n.4431G>A
NR_104390.2:n.4313G>A
NR_104391.1:n.4431G>A
NR_104391.2:n.4313G>A
NR_104392.1:n.4431G>A
NR_104392.2:n.4313G>A
NR_104393.1:n.4431G>A
NR_104393.2:n.4313G>A
NR_104394.1:n.4431G>A
NR_104394.2:n.4313G>A
NR_104395.1:n.4431G>A
NR_104395.2:n.4313G>A
ENST00000276072.7:c.4355G>A	ENSP00000276072.3:p.Arg1452His
ENST00000276072.8:c.889G>A
ENST00000276072.9:c.3581G>A	ENSP00000276072.5:p.Arg1194His
ENST00000373775.8:c.256G>A
ENST00000373790.8:c.4292G>A	ENSP00000362895.4:p.Arg1431His
ENST00000373790.9:c.4232G>A	ENSP00000362895.5:p.Arg1411His
ENST00000423759.5:c.4355G>A	ENSP00000406549.1:p.Arg1452His
ENST00000437147.7:c.256G>A
ENST00000437147.8:c.256G>A
ENST00000461764.6:c.256G>A
ENST00000463163.5:c.289G>A
ENST00000485087.6:c.256G>A
ENST00000682124.1:c.256G>A
ENST00000683202.1:c.4295G>A	ENSP00000507781.1:p.Arg1432His
ENST00000683358.1:c.256G>A
ENST00000683668.1:c.3581G>A	ENSP00000507280.1:p.Arg1194His
ENST00000683782.1:c.4295G>A	ENSP00000506996.1:p.Arg1432His
XM_005262295.1:c.4355G>A	XP_005262352.1:p.Arg1452His
XM_005262296.1:c.4352G>A	XP_005262353.1:p.Arg1451His
XM_005262297.3:c.4292G>A	XP_005262354.1:p.Arg1431His
XM_005262297.4:c.4292G>A	XP_005262354.1:p.Arg1431His
XM_006724682.2:c.3974G>A	XP_006724745.1:p.Arg1325His
XM_011531016.1:c.4355G>A	XP_011529318.1:p.Arg1452His
XM_024452429.1:c.3974G>A	XP_024308197.1:p.Arg1325His
XM_024452430.1:c.4355G>A	XP_024308198.1:p.Arg1452His
XR_938407.1:n.4365G>A