Canonical Allele Identifier: CA413531886

Gene: TAF1

Linked Data

• MyVariant Identifiers: chrX:g.70618500G>C (hg19) ; chrX:g.71398650G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71398650G>C , CM000685.2:g.71398650G>C	GRCh38
NC_000023.10:g.70618500G>C , CM000685.1:g.70618500G>C	GRCh37
NC_000023.9:g.70535225G>C	NCBI36
NG_012771.2:g.37387G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276072.9:c.2985G>C	ENSP00000276072.5:p.Arg995Ser
ENST00000483985.3:c.614G>C
ENST00000683202.1:c.3699G>C	ENSP00000507781.1:p.Arg1233Ser
ENST00000683668.1:c.2985G>C	ENSP00000507280.1:p.Arg995Ser
ENST00000683782.1:c.3699G>C	ENSP00000506996.1:p.Arg1233Ser
ENST00000276072.8:c.293G>C
ENST00000373790.9:c.3636G>C	ENSP00000362895.5:p.Arg1212Ser
ENST00000423759.6:c.3699G>C MANE Select	ENSP00000406549.2:p.Arg1233Ser
ENST00000276072.7:c.3759G>C	ENSP00000276072.3:p.Arg1253Ser
ENST00000373790.8:c.3696G>C	ENSP00000362895.4:p.Arg1232Ser
ENST00000423759.5:c.3759G>C	ENSP00000406549.1:p.Arg1253Ser
ENST00000483985.2:c.428G>C
NM_001286074.1:c.3759G>C	NP_001273003.1:p.Arg1253Ser
NM_004606.4:c.3759G>C	NP_004597.2:p.Arg1253Ser
NM_138923.3:c.3696G>C	NP_620278.1:p.Arg1232Ser
NR_104387.1:n.3835G>C
NR_104388.1:n.3835G>C
NR_104389.1:n.3835G>C
NR_104390.1:n.3835G>C
NR_104391.1:n.3835G>C
NR_104392.1:n.3835G>C
NR_104393.1:n.3835G>C
NR_104394.1:n.3835G>C
NR_104395.1:n.3835G>C
XM_005262295.1:c.3759G>C	XP_005262352.1:p.Arg1253Ser
XM_005262296.1:c.3756G>C	XP_005262353.1:p.Arg1252Ser
XM_005262297.3:c.3696G>C	XP_005262354.1:p.Arg1232Ser
XM_006724682.2:c.3378G>C	XP_006724745.1:p.Arg1126Ser
XM_011531016.1:c.3759G>C	XP_011529318.1:p.Arg1253Ser
XR_938407.1:n.3769G>C
XM_005262297.4:c.3696G>C	XP_005262354.1:p.Arg1232Ser
XM_024452429.1:c.3378G>C	XP_024308197.1:p.Arg1126Ser
XM_024452430.1:c.3759G>C	XP_024308198.1:p.Arg1253Ser
NM_001286074.2:c.3699G>C	NP_001273003.2:p.Arg1233Ser
NM_004606.5:c.3699G>C MANE Select	NP_004597.3:p.Arg1233Ser
NM_138923.4:c.3636G>C	NP_620278.2:p.Arg1212Ser
NR_104387.2:n.3717G>C
NR_104388.2:n.3717G>C
NR_104389.2:n.3717G>C
NR_104390.2:n.3717G>C
NR_104391.2:n.3717G>C
NR_104392.2:n.3717G>C
NR_104393.2:n.3717G>C
NR_104394.2:n.3717G>C
NR_104395.2:n.3717G>C