Canonical Allele Identifier: CA2436444709

Gene: TAF1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71382813A= , CM000685.2:g.71382813A=	GRCh38
NC_000023.10:g.70602663A= , CM000685.1:g.70602663A=	GRCh37
NC_000023.9:g.70519388A=	NCBI36
NG_012771.2:g.21550A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276072.9:c.1004A=	ENSP00000276072.5:p.Tyr335=
ENST00000683202.1:c.1718A=	ENSP00000507781.1:p.Tyr573=
ENST00000683668.1:c.1004A=	ENSP00000507280.1:p.Tyr335=
ENST00000683715.1:c.1299A=
ENST00000683782.1:c.1718A=	ENSP00000506996.1:p.Tyr573=
ENST00000373790.9:c.1655A=	ENSP00000362895.5:p.Tyr552=
ENST00000423759.6:c.1718A= MANE Select	ENSP00000406549.2:p.Tyr573=
ENST00000276072.7:c.1778A=	ENSP00000276072.3:p.Tyr593=
ENST00000373790.8:c.1715A=	ENSP00000362895.4:p.Tyr572=
ENST00000423759.5:c.1778A=	ENSP00000406549.1:p.Tyr593=
NM_001286074.1:c.1778A=	NP_001273003.1:p.Tyr593=
NM_004606.4:c.1778A=	NP_004597.2:p.Tyr593=
NM_138923.3:c.1715A=	NP_620278.1:p.Tyr572=
NR_104387.1:n.1854A=
NR_104388.1:n.1854A=
NR_104389.1:n.1854A=
NR_104390.1:n.1854A=
NR_104391.1:n.1854A=
NR_104392.1:n.1854A=
NR_104393.1:n.1854A=
NR_104394.1:n.1854A=
NR_104395.1:n.1854A=
XM_005262295.1:c.1778A=	XP_005262352.1:p.Tyr593=
XM_005262296.1:c.1778A=	XP_005262353.1:p.Tyr593=
XM_005262297.3:c.1715A=	XP_005262354.1:p.Tyr572=
XM_005262300.1:c.1778A=	XP_005262357.1:p.Tyr593=
XM_006724682.2:c.1397A=	XP_006724745.1:p.Tyr466=
XM_011531016.1:c.1778A=	XP_011529318.1:p.Tyr593=
XR_938407.1:n.1788A=
XM_005262297.4:c.1715A=	XP_005262354.1:p.Tyr572=
XM_005262300.2:c.1778A=	XP_005262357.1:p.Tyr593=
XM_024452429.1:c.1397A=	XP_024308197.1:p.Tyr466=
XM_024452430.1:c.1778A=	XP_024308198.1:p.Tyr593=
NM_001286074.2:c.1718A=	NP_001273003.2:p.Tyr573=
NM_004606.5:c.1718A= MANE Select	NP_004597.3:p.Tyr573=
NM_138923.4:c.1655A=	NP_620278.2:p.Tyr552=
NR_104387.2:n.1736A=
NR_104388.2:n.1736A=
NR_104389.2:n.1736A=
NR_104390.2:n.1736A=
NR_104391.2:n.1736A=
NR_104392.2:n.1736A=
NR_104393.2:n.1736A=
NR_104394.2:n.1736A=
NR_104395.2:n.1736A=