Canonical Allele Identifier: CA413502631

Gene: TAF1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71366402T>G , CM000685.2:g.71366402T>G	GRCh38
NC_000023.10:g.70586252T>G , CM000685.1:g.70586252T>G	GRCh37
NC_000023.9:g.70502977T>G	NCBI36
NG_012771.2:g.5139T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483365.2:n.139T>G
ENST00000683202.1:c.28T>G	ENSP00000507781.1:p.Ser10Ala
ENST00000683352.1:n.98T>G
ENST00000683782.1:c.28T>G	ENSP00000506996.1:p.Ser10Ala
ENST00000373790.9:c.28T>G	ENSP00000362895.5:p.Ser10Ala
ENST00000423759.6:c.28T>G MANE Select	ENSP00000406549.2:p.Ser10Ala
ENST00000276072.7:c.88T>G	ENSP00000276072.3:p.Ser30Ala
ENST00000373790.8:c.88T>G	ENSP00000362895.4:p.Ser30Ala
ENST00000423759.5:c.88T>G	ENSP00000406549.1:p.Ser30Ala
NM_001286074.1:c.88T>G	NP_001273003.1:p.Ser30Ala
NM_004606.4:c.88T>G	NP_004597.2:p.Ser30Ala
NM_138923.3:c.88T>G	NP_620278.1:p.Ser30Ala
NR_104387.1:n.164T>G
NR_104388.1:n.164T>G
NR_104389.1:n.164T>G
NR_104390.1:n.164T>G
NR_104391.1:n.164T>G
NR_104392.1:n.164T>G
NR_104393.1:n.164T>G
NR_104394.1:n.164T>G
NR_104395.1:n.164T>G
XM_005262295.1:c.88T>G	XP_005262352.1:p.Ser30Ala
XM_005262296.1:c.88T>G	XP_005262353.1:p.Ser30Ala
XM_005262297.3:c.88T>G	XP_005262354.1:p.Ser30Ala
XM_005262300.1:c.88T>G	XP_005262357.1:p.Ser30Ala
XM_011531016.1:c.88T>G	XP_011529318.1:p.Ser30Ala
XR_938407.1:n.98T>G
XM_005262297.4:c.88T>G	XP_005262354.1:p.Ser30Ala
XM_005262300.2:c.88T>G	XP_005262357.1:p.Ser30Ala
XM_024452429.1:c.-281T>G	XP_024308197.1:n.-281T>G
XM_024452430.1:c.88T>G	XP_024308198.1:p.Ser30Ala
NM_001286074.2:c.28T>G	NP_001273003.2:p.Ser10Ala
NM_004606.5:c.28T>G MANE Select	NP_004597.3:p.Ser10Ala
NM_138923.4:c.28T>G	NP_620278.2:p.Ser10Ala
NR_104387.2:n.46T>G
NR_104388.2:n.46T>G
NR_104389.2:n.46T>G
NR_104390.2:n.46T>G
NR_104391.2:n.46T>G
NR_104392.2:n.46T>G
NR_104393.2:n.46T>G
NR_104394.2:n.46T>G
NR_104395.2:n.46T>G