Canonical Allele Identifier: CA413514173

Gene: TAF1

Linked Data

• MyVariant Identifiers: chrX:g.70602682G>C (hg19) ; chrX:g.71382832G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71382832G>C , CM000685.2:g.71382832G>C	GRCh38
NC_000023.10:g.70602682G>C , CM000685.1:g.70602682G>C	GRCh37
NC_000023.9:g.70519407G>C	NCBI36
NG_012771.2:g.21569G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276072.9:c.1023G>C	ENSP00000276072.5:p.Gln341His
ENST00000683202.1:c.1737G>C	ENSP00000507781.1:p.Gln579His
ENST00000683668.1:c.1023G>C	ENSP00000507280.1:p.Gln341His
ENST00000683715.1:c.1318G>C
ENST00000683782.1:c.1737G>C	ENSP00000506996.1:p.Gln579His
ENST00000373790.9:c.1674G>C	ENSP00000362895.5:p.Gln558His
ENST00000423759.6:c.1737G>C MANE Select	ENSP00000406549.2:p.Gln579His
ENST00000276072.7:c.1797G>C	ENSP00000276072.3:p.Gln599His
ENST00000373790.8:c.1734G>C	ENSP00000362895.4:p.Gln578His
ENST00000423759.5:c.1797G>C	ENSP00000406549.1:p.Gln599His
NM_001286074.1:c.1797G>C	NP_001273003.1:p.Gln599His
NM_004606.4:c.1797G>C	NP_004597.2:p.Gln599His
NM_138923.3:c.1734G>C	NP_620278.1:p.Gln578His
NR_104387.1:n.1873G>C
NR_104388.1:n.1873G>C
NR_104389.1:n.1873G>C
NR_104390.1:n.1873G>C
NR_104391.1:n.1873G>C
NR_104392.1:n.1873G>C
NR_104393.1:n.1873G>C
NR_104394.1:n.1873G>C
NR_104395.1:n.1873G>C
XM_005262295.1:c.1797G>C	XP_005262352.1:p.Gln599His
XM_005262296.1:c.1797G>C	XP_005262353.1:p.Gln599His
XM_005262297.3:c.1734G>C	XP_005262354.1:p.Gln578His
XM_005262300.1:c.1797G>C	XP_005262357.1:p.Gln599His
XM_006724682.2:c.1416G>C	XP_006724745.1:p.Gln472His
XM_011531016.1:c.1797G>C	XP_011529318.1:p.Gln599His
XR_938407.1:n.1807G>C
XM_005262297.4:c.1734G>C	XP_005262354.1:p.Gln578His
XM_005262300.2:c.1797G>C	XP_005262357.1:p.Gln599His
XM_024452429.1:c.1416G>C	XP_024308197.1:p.Gln472His
XM_024452430.1:c.1797G>C	XP_024308198.1:p.Gln599His
NM_001286074.2:c.1737G>C	NP_001273003.2:p.Gln579His
NM_004606.5:c.1737G>C MANE Select	NP_004597.3:p.Gln579His
NM_138923.4:c.1674G>C	NP_620278.2:p.Gln558His
NR_104387.2:n.1755G>C
NR_104388.2:n.1755G>C
NR_104389.2:n.1755G>C
NR_104390.2:n.1755G>C
NR_104391.2:n.1755G>C
NR_104392.2:n.1755G>C
NR_104393.2:n.1755G>C
NR_104394.2:n.1755G>C
NR_104395.2:n.1755G>C