Canonical Allele Identifier: CA413531486

Gene: TAF1

Linked Data

• gnomAD v4: X-71398594-G-C
• MyVariant Identifiers: chrX:g.70618444G>C (hg19) ; chrX:g.71398594G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71398594G>C , CM000685.2:g.71398594G>C	GRCh38
NC_000023.10:g.70618444G>C , CM000685.1:g.70618444G>C	GRCh37
NC_000023.9:g.70535169G>C	NCBI36
NG_012771.2:g.37331G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276072.9:c.2929G>C	ENSP00000276072.5:p.Glu977Gln
ENST00000483985.3:c.558G>C
ENST00000683202.1:c.3643G>C	ENSP00000507781.1:p.Glu1215Gln
ENST00000683668.1:c.2929G>C	ENSP00000507280.1:p.Glu977Gln
ENST00000683782.1:c.3643G>C	ENSP00000506996.1:p.Glu1215Gln
ENST00000276072.8:c.237G>C
ENST00000373790.9:c.3580G>C	ENSP00000362895.5:p.Glu1194Gln
ENST00000423759.6:c.3643G>C MANE Select	ENSP00000406549.2:p.Glu1215Gln
ENST00000276072.7:c.3703G>C	ENSP00000276072.3:p.Glu1235Gln
ENST00000373790.8:c.3640G>C	ENSP00000362895.4:p.Glu1214Gln
ENST00000423759.5:c.3703G>C	ENSP00000406549.1:p.Glu1235Gln
ENST00000483985.2:c.372G>C
NM_001286074.1:c.3703G>C	NP_001273003.1:p.Glu1235Gln
NM_004606.4:c.3703G>C	NP_004597.2:p.Glu1235Gln
NM_138923.3:c.3640G>C	NP_620278.1:p.Glu1214Gln
NR_104387.1:n.3779G>C
NR_104388.1:n.3779G>C
NR_104389.1:n.3779G>C
NR_104390.1:n.3779G>C
NR_104391.1:n.3779G>C
NR_104392.1:n.3779G>C
NR_104393.1:n.3779G>C
NR_104394.1:n.3779G>C
NR_104395.1:n.3779G>C
XM_005262295.1:c.3703G>C	XP_005262352.1:p.Glu1235Gln
XM_005262296.1:c.3700G>C	XP_005262353.1:p.Glu1234Gln
XM_005262297.3:c.3640G>C	XP_005262354.1:p.Glu1214Gln
XM_006724682.2:c.3322G>C	XP_006724745.1:p.Glu1108Gln
XM_011531016.1:c.3703G>C	XP_011529318.1:p.Glu1235Gln
XR_938407.1:n.3713G>C
XM_005262297.4:c.3640G>C	XP_005262354.1:p.Glu1214Gln
XM_024452429.1:c.3322G>C	XP_024308197.1:p.Glu1108Gln
XM_024452430.1:c.3703G>C	XP_024308198.1:p.Glu1235Gln
NM_001286074.2:c.3643G>C	NP_001273003.2:p.Glu1215Gln
NM_004606.5:c.3643G>C MANE Select	NP_004597.3:p.Glu1215Gln
NM_138923.4:c.3580G>C	NP_620278.2:p.Glu1194Gln
NR_104387.2:n.3661G>C
NR_104388.2:n.3661G>C
NR_104389.2:n.3661G>C
NR_104390.2:n.3661G>C
NR_104391.2:n.3661G>C
NR_104392.2:n.3661G>C
NR_104393.2:n.3661G>C
NR_104394.2:n.3661G>C
NR_104395.2:n.3661G>C