Canonical Allele Identifier: CA2759854500

Gene: TP63

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189789739_189789740insT , CM000665.2:g.189789739_189789740insT	GRCh38
NC_000003.11:g.189507528_189507529insT , CM000665.1:g.189507528_189507529insT	GRCh37
NC_000003.10:g.190990222_190990223insT	NCBI36
NG_007550.1:g.163313_163314insT
NG_007550.2:g.163313_163314insT
NG_007550.3:g.197994_197995insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264731.8:c.325-18533_325-18532insT MANE Select	ENSP00000264731.3:n.325-18533_325-18532insT
ENST00000354600.10:c.-62_-61insT MANE Plus Clinical	ENSP00000346614.5:n.-62_-61insT
ENST00000264731.7:c.325-18533_325-18532insT	ENSP00000264731.3:n.325-18533_325-18532insT
ENST00000320472.9:c.325-18533_325-18532insT	ENSP00000317510.5:n.325-18533_325-18532insT
ENST00000354600.9:c.-62_-61insT	ENSP00000346614.5:n.-62_-61insT
ENST00000392460.7:c.325-18533_325-18532insT	ENSP00000376253.3:n.325-18533_325-18532insT
ENST00000418709.6:c.325-18533_325-18532insT	ENSP00000407144.2:n.325-18533_325-18532insT
ENST00000434928.5:c.-62_-61insT	ENSP00000401661.1:n.-62_-61insT
ENST00000440651.6:c.325-18533_325-18532insT	ENSP00000394337.2:n.325-18533_325-18532insT
ENST00000460036.1:n.45_46insT
NM_001114978.1:c.325-18533_325-18532insT	NP_001108450.1:n.325-18533_325-18532insT
NM_001114979.1:c.325-18533_325-18532insT	NP_001108451.1:n.325-18533_325-18532insT
NM_001114980.1:c.-62_-61insT	NP_001108452.1:n.-62_-61insT
NM_001114981.1:c.-62_-61insT	NP_001108453.1:n.-62_-61insT
NM_001114982.1:c.-62_-61insT	NP_001108454.1:n.-62_-61insT
NM_003722.4:c.325-18533_325-18532insT	NP_003713.3:n.325-18533_325-18532insT
XM_005247843.2:c.325-18533_325-18532insT	XP_005247900.1:n.325-18533_325-18532insT
XM_005247844.3:c.274-18533_274-18532insT	XP_005247901.1:n.274-18533_274-18532insT
XM_005247846.2:c.325-18533_325-18532insT	XP_005247903.1:n.325-18533_325-18532insT
XM_011513251.1:c.322-18533_322-18532insT	XP_011511553.1:n.322-18533_322-18532insT
XM_011513252.1:c.319-18533_319-18532insT	XP_011511554.1:n.319-18533_319-18532insT
XM_011513253.1:c.286-18533_286-18532insT	XP_011511555.1:n.286-18533_286-18532insT
NM_001329144.1:c.325-18533_325-18532insT	NP_001316073.1:n.325-18533_325-18532insT
NM_001329145.1:c.-62_-61insT	NP_001316074.1:n.-62_-61insT
NM_001329146.1:c.-62_-61insT	NP_001316075.1:n.-62_-61insT
NM_001329148.1:c.325-18533_325-18532insT	NP_001316077.1:n.325-18533_325-18532insT
NM_001329149.1:c.-62_-61insT	NP_001316078.1:n.-62_-61insT
NM_001329150.1:c.-62_-61insT	NP_001316079.1:n.-62_-61insT
NM_001329964.1:c.319-18533_319-18532insT	NP_001316893.1:n.319-18533_319-18532insT
NM_003722.5:c.325-18533_325-18532insT MANE Select	NP_003713.3:n.325-18533_325-18532insT
NM_001114978.2:c.325-18533_325-18532insT	NP_001108450.1:n.325-18533_325-18532insT
NM_001114979.2:c.325-18533_325-18532insT	NP_001108451.1:n.325-18533_325-18532insT
NM_001114980.2:c.-62_-61insT MANE Plus Clinical	NP_001108452.1:n.-62_-61insT
NM_001114981.2:c.-62_-61insT	NP_001108453.1:n.-62_-61insT
NM_001114982.2:c.-62_-61insT	NP_001108454.1:n.-62_-61insT
NM_001329144.2:c.325-18533_325-18532insT	NP_001316073.1:n.325-18533_325-18532insT
NM_001329145.2:c.-62_-61insT	NP_001316074.1:n.-62_-61insT
NM_001329146.2:c.-62_-61insT	NP_001316075.1:n.-62_-61insT
NM_001329148.2:c.325-18533_325-18532insT	NP_001316077.1:n.325-18533_325-18532insT
NM_001329149.2:c.-62_-61insT	NP_001316078.1:n.-62_-61insT
NM_001329150.2:c.-62_-61insT	NP_001316079.1:n.-62_-61insT
NM_001329964.2:c.319-18533_319-18532insT	NP_001316893.1:n.319-18533_319-18532insT