Canonical Allele Identifier: CA413514474

Gene: TAF1

Linked Data

• MyVariant Identifiers: chrX:g.70602870G>C (hg19) ; chrX:g.71383020G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71383020G>C , CM000685.2:g.71383020G>C	GRCh38
NC_000023.10:g.70602870G>C , CM000685.1:g.70602870G>C	GRCh37
NC_000023.9:g.70519595G>C	NCBI36
NG_012771.2:g.21757G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276072.9:c.1089G>C	ENSP00000276072.5:p.Gln363His
ENST00000683202.1:c.1803G>C	ENSP00000507781.1:p.Gln601His
ENST00000683668.1:c.1089G>C	ENSP00000507280.1:p.Gln363His
ENST00000683715.1:c.1384G>C
ENST00000683782.1:c.1803G>C	ENSP00000506996.1:p.Gln601His
ENST00000373790.9:c.1740G>C	ENSP00000362895.5:p.Gln580His
ENST00000423759.6:c.1803G>C MANE Select	ENSP00000406549.2:p.Gln601His
ENST00000276072.7:c.1863G>C	ENSP00000276072.3:p.Gln621His
ENST00000373790.8:c.1800G>C	ENSP00000362895.4:p.Gln600His
ENST00000423759.5:c.1863G>C	ENSP00000406549.1:p.Gln621His
NM_001286074.1:c.1863G>C	NP_001273003.1:p.Gln621His
NM_004606.4:c.1863G>C	NP_004597.2:p.Gln621His
NM_138923.3:c.1800G>C	NP_620278.1:p.Gln600His
NR_104387.1:n.1939G>C
NR_104388.1:n.1939G>C
NR_104389.1:n.1939G>C
NR_104390.1:n.1939G>C
NR_104391.1:n.1939G>C
NR_104392.1:n.1939G>C
NR_104393.1:n.1939G>C
NR_104394.1:n.1939G>C
NR_104395.1:n.1939G>C
XM_005262295.1:c.1863G>C	XP_005262352.1:p.Gln621His
XM_005262296.1:c.1863G>C	XP_005262353.1:p.Gln621His
XM_005262297.3:c.1800G>C	XP_005262354.1:p.Gln600His
XM_005262300.1:c.1863G>C	XP_005262357.1:p.Gln621His
XM_006724682.2:c.1482G>C	XP_006724745.1:p.Gln494His
XM_011531016.1:c.1863G>C	XP_011529318.1:p.Gln621His
XR_938407.1:n.1873G>C
XM_005262297.4:c.1800G>C	XP_005262354.1:p.Gln600His
XM_005262300.2:c.1863G>C	XP_005262357.1:p.Gln621His
XM_024452429.1:c.1482G>C	XP_024308197.1:p.Gln494His
XM_024452430.1:c.1863G>C	XP_024308198.1:p.Gln621His
NM_001286074.2:c.1803G>C	NP_001273003.2:p.Gln601His
NM_004606.5:c.1803G>C MANE Select	NP_004597.3:p.Gln601His
NM_138923.4:c.1740G>C	NP_620278.2:p.Gln580His
NR_104387.2:n.1821G>C
NR_104388.2:n.1821G>C
NR_104389.2:n.1821G>C
NR_104390.2:n.1821G>C
NR_104391.2:n.1821G>C
NR_104392.2:n.1821G>C
NR_104393.2:n.1821G>C
NR_104394.2:n.1821G>C
NR_104395.2:n.1821G>C