Canonical Allele Identifier: CA413525204

Gene: TAF1

Linked Data

• MyVariant Identifiers: chrX:g.70612545C>G (hg19) ; chrX:g.71392695C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71392695C>G , CM000685.2:g.71392695C>G	GRCh38
NC_000023.10:g.70612545C>G , CM000685.1:g.70612545C>G	GRCh37
NC_000023.9:g.70529270C>G	NCBI36
NG_012771.2:g.31432C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000276072.9:c.2194C>G	ENSP00000276072.5:p.Pro732Ala
ENST00000683202.1:c.2908C>G	ENSP00000507781.1:p.Pro970Ala
ENST00000683668.1:c.2194C>G	ENSP00000507280.1:p.Pro732Ala
ENST00000683715.1:c.2489C>G
ENST00000683782.1:c.2908C>G	ENSP00000506996.1:p.Pro970Ala
ENST00000373790.9:c.2845C>G	ENSP00000362895.5:p.Pro949Ala
ENST00000423759.6:c.2908C>G MANE Select	ENSP00000406549.2:p.Pro970Ala
ENST00000276072.7:c.2968C>G	ENSP00000276072.3:p.Pro990Ala
ENST00000373790.8:c.2905C>G	ENSP00000362895.4:p.Pro969Ala
ENST00000423759.5:c.2968C>G	ENSP00000406549.1:p.Pro990Ala
NM_001286074.1:c.2968C>G	NP_001273003.1:p.Pro990Ala
NM_004606.4:c.2968C>G	NP_004597.2:p.Pro990Ala
NM_138923.3:c.2905C>G	NP_620278.1:p.Pro969Ala
NR_104387.1:n.3044C>G
NR_104388.1:n.3044C>G
NR_104389.1:n.3044C>G
NR_104390.1:n.3044C>G
NR_104391.1:n.3044C>G
NR_104392.1:n.3044C>G
NR_104393.1:n.3044C>G
NR_104394.1:n.3044C>G
NR_104395.1:n.3044C>G
XM_005262295.1:c.2968C>G	XP_005262352.1:p.Pro990Ala
XM_005262296.1:c.2968C>G	XP_005262353.1:p.Pro990Ala
XM_005262297.3:c.2905C>G	XP_005262354.1:p.Pro969Ala
XM_005262300.1:c.2968C>G	XP_005262357.1:p.Pro990Ala
XM_006724682.2:c.2587C>G	XP_006724745.1:p.Pro863Ala
XM_011531016.1:c.2968C>G	XP_011529318.1:p.Pro990Ala
XR_938407.1:n.2978C>G
XM_005262297.4:c.2905C>G	XP_005262354.1:p.Pro969Ala
XM_005262300.2:c.2968C>G	XP_005262357.1:p.Pro990Ala
XM_024452429.1:c.2587C>G	XP_024308197.1:p.Pro863Ala
XM_024452430.1:c.2968C>G	XP_024308198.1:p.Pro990Ala
NM_001286074.2:c.2908C>G	NP_001273003.2:p.Pro970Ala
NM_004606.5:c.2908C>G MANE Select	NP_004597.3:p.Pro970Ala
NM_138923.4:c.2845C>G	NP_620278.2:p.Pro949Ala
NR_104387.2:n.2926C>G
NR_104388.2:n.2926C>G
NR_104389.2:n.2926C>G
NR_104390.2:n.2926C>G
NR_104391.2:n.2926C>G
NR_104392.2:n.2926C>G
NR_104393.2:n.2926C>G
NR_104394.2:n.2926C>G
NR_104395.2:n.2926C>G