Canonical Allele Identifier: CA645604548
Gene: TAF1 HGNC NCBI

Linked Data

COSMIC: COSM241834

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71382812_71382828del , CM000685.2:g.71382812_71382828del GRCh38
NC_000023.10:g.70602662_70602678del , CM000685.1:g.70602662_70602678del GRCh37
NC_000023.9:g.70519387_70519403del NCBI36
NG_012771.2:g.21549_21565del

Transcript Alleles

HGVS Amino-acid Change
ENST00000276072.9:c.1003_1019del ENSP00000276072.5:p.Tyr335ThrfsTer?
ENST00000683202.1:c.1717_1733del ENSP00000507781.1:p.Tyr573ThrfsTer?
ENST00000683668.1:c.1003_1019del ENSP00000507280.1:p.Tyr335ThrfsTer?
ENST00000683715.1:c.1298_1314del
ENST00000683782.1:c.1717_1733del ENSP00000506996.1:p.Tyr573ThrfsTer?
ENST00000373790.9:c.1654_1670del ENSP00000362895.5:p.Tyr552ThrfsTer?
ENST00000423759.6:c.1717_1733del MANE Select ENSP00000406549.2:p.Tyr573ThrfsTer?
ENST00000276072.7:c.1777_1793del ENSP00000276072.3:p.Tyr593ThrfsTer?
ENST00000373790.8:c.1714_1730del ENSP00000362895.4:p.Tyr572ThrfsTer?
ENST00000423759.5:c.1777_1793del ENSP00000406549.1:p.Tyr593ThrfsTer?
NM_001286074.1:c.1777_1793del NP_001273003.1:p.Tyr593ThrfsTer?
NM_004606.4:c.1777_1793del NP_004597.2:p.Tyr593ThrfsTer?
NM_138923.3:c.1714_1730del NP_620278.1:p.Tyr572ThrfsTer?
NR_104387.1:n.1853_1869del
NR_104388.1:n.1853_1869del
NR_104389.1:n.1853_1869del
NR_104390.1:n.1853_1869del
NR_104391.1:n.1853_1869del
NR_104392.1:n.1853_1869del
NR_104393.1:n.1853_1869del
NR_104394.1:n.1853_1869del
NR_104395.1:n.1853_1869del
XM_005262295.1:c.1777_1793del XP_005262352.1:p.Tyr593ThrfsTer?
XM_005262296.1:c.1777_1793del XP_005262353.1:p.Tyr593ThrfsTer?
XM_005262297.3:c.1714_1730del XP_005262354.1:p.Tyr572ThrfsTer?
XM_005262300.1:c.1777_1793del XP_005262357.1:p.Tyr593ThrfsTer?
XM_006724682.2:c.1396_1412del XP_006724745.1:p.Tyr466ThrfsTer?
XM_011531016.1:c.1777_1793del XP_011529318.1:p.Tyr593ThrfsTer?
XR_938407.1:n.1787_1803del
XM_005262297.4:c.1714_1730del XP_005262354.1:p.Tyr572ThrfsTer?
XM_005262300.2:c.1777_1793del XP_005262357.1:p.Tyr593ThrfsTer?
XM_024452429.1:c.1396_1412del XP_024308197.1:p.Tyr466ThrfsTer?
XM_024452430.1:c.1777_1793del XP_024308198.1:p.Tyr593ThrfsTer?
NM_001286074.2:c.1717_1733del NP_001273003.2:p.Tyr573ThrfsTer?
NM_004606.5:c.1717_1733del MANE Select NP_004597.3:p.Tyr573ThrfsTer?
NM_138923.4:c.1654_1670del NP_620278.2:p.Tyr552ThrfsTer?
NR_104387.2:n.1735_1751del
NR_104388.2:n.1735_1751del
NR_104389.2:n.1735_1751del
NR_104390.2:n.1735_1751del
NR_104391.2:n.1735_1751del
NR_104392.2:n.1735_1751del
NR_104393.2:n.1735_1751del
NR_104394.2:n.1735_1751del
NR_104395.2:n.1735_1751del