Canonical Allele Identifier: CA1428533829

Gene: TP63

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189891172_189891174delinsCAT , CM000665.2:g.189891172_189891174delinsCAT	GRCh38
NC_000003.11:g.189608961_189608963delinsCAT , CM000665.1:g.189608961_189608963delinsCAT	GRCh37
NC_000003.10:g.191091655_191091657delinsCAT	NCBI36
NG_007550.1:g.264746_264748delinsCAT
NG_007550.2:g.264746_264748delinsCAT
NG_007550.3:g.299427_299429delinsCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264731.8:c.1746+290_1746+292delinsCAT MANE Select	ENSP00000264731.3:n.1746+290_1746+292delinsCAT
ENST00000354600.10:c.1464+290_1464+292delinsCAT MANE Plus Clinical	ENSP00000346614.5:n.1464+290_1464+292delinsCAT
ENST00000264731.7:c.1746+290_1746+292delinsCAT	ENSP00000264731.3:n.1746+290_1746+292delinsCAT
ENST00000320472.9:c.1508-3034_1508-3032delinsCAT	ENSP00000317510.5:n.1508-3034_1508-3032delinsCAT
ENST00000354600.9:c.1464+290_1464+292delinsCAT	ENSP00000346614.5:n.1464+290_1464+292delinsCAT
ENST00000392460.7:c.1652+1688_1652+1690delinsCAT	ENSP00000376253.3:n.1652+1688_1652+1690delinsCAT
ENST00000392461.7:c.1226-3034_1226-3032delinsCAT	ENSP00000376254.3:n.1226-3034_1226-3032delinsCAT
ENST00000392463.6:c.1370+1688_1370+1690delinsCAT	ENSP00000376256.2:n.1370+1688_1370+1690delinsCAT
ENST00000440651.6:c.1734+290_1734+292delinsCAT	ENSP00000394337.2:n.1734+290_1734+292delinsCAT
ENST00000449992.5:c.1209+290_1209+292delinsCAT	ENSP00000387839.1:n.1209+290_1209+292delinsCAT
ENST00000456148.1:c.1452+290_1452+292delinsCAT	ENSP00000389485.1:n.1452+290_1452+292delinsCAT
NM_001114978.1:c.1652+1688_1652+1690delinsCAT	NP_001108450.1:n.1652+1688_1652+1690delinsCAT
NM_001114980.1:c.1464+290_1464+292delinsCAT	NP_001108452.1:n.1464+290_1464+292delinsCAT
NM_001114981.1:c.1370+1688_1370+1690delinsCAT	NP_001108453.1:n.1370+1688_1370+1690delinsCAT
NM_003722.4:c.1746+290_1746+292delinsCAT	NP_003713.3:n.1746+290_1746+292delinsCAT
XM_005247843.2:c.1734+290_1734+292delinsCAT	XP_005247900.1:n.1734+290_1734+292delinsCAT
XM_005247844.3:c.1695+290_1695+292delinsCAT	XP_005247901.1:n.1695+290_1695+292delinsCAT
XM_011513251.1:c.1743+290_1743+292delinsCAT	XP_011511553.1:n.1743+290_1743+292delinsCAT
XM_011513252.1:c.1740+290_1740+292delinsCAT	XP_011511554.1:n.1740+290_1740+292delinsCAT
XM_011513253.1:c.1707+290_1707+292delinsCAT	XP_011511555.1:n.1707+290_1707+292delinsCAT
NM_001329144.1:c.1508-3034_1508-3032delinsCAT	NP_001316073.1:n.1508-3034_1508-3032delinsCAT
NM_001329145.1:c.1226-3034_1226-3032delinsCAT	NP_001316074.1:n.1226-3034_1226-3032delinsCAT
NM_001329146.1:c.1209+290_1209+292delinsCAT	NP_001316075.1:n.1209+290_1209+292delinsCAT
NM_001329148.1:c.1734+290_1734+292delinsCAT	NP_001316077.1:n.1734+290_1734+292delinsCAT
NM_001329149.1:c.1214-3034_1214-3032delinsCAT	NP_001316078.1:n.1214-3034_1214-3032delinsCAT
NM_001329150.1:c.959-3034_959-3032delinsCAT	NP_001316079.1:n.959-3034_959-3032delinsCAT
NM_001329964.1:c.1740+290_1740+292delinsCAT	NP_001316893.1:n.1740+290_1740+292delinsCAT
NM_003722.5:c.1746+290_1746+292delinsCAT MANE Select	NP_003713.3:n.1746+290_1746+292delinsCAT
NM_001114978.2:c.1652+1688_1652+1690delinsCAT	NP_001108450.1:n.1652+1688_1652+1690delinsCAT
NM_001114980.2:c.1464+290_1464+292delinsCAT MANE Plus Clinical	NP_001108452.1:n.1464+290_1464+292delinsCAT
NM_001114981.2:c.1370+1688_1370+1690delinsCAT	NP_001108453.1:n.1370+1688_1370+1690delinsCAT
NM_001329144.2:c.1508-3034_1508-3032delinsCAT	NP_001316073.1:n.1508-3034_1508-3032delinsCAT
NM_001329145.2:c.1226-3034_1226-3032delinsCAT	NP_001316074.1:n.1226-3034_1226-3032delinsCAT
NM_001329146.2:c.1209+290_1209+292delinsCAT	NP_001316075.1:n.1209+290_1209+292delinsCAT
NM_001329148.2:c.1734+290_1734+292delinsCAT	NP_001316077.1:n.1734+290_1734+292delinsCAT
NM_001329149.2:c.1214-3034_1214-3032delinsCAT	NP_001316078.1:n.1214-3034_1214-3032delinsCAT
NM_001329150.2:c.959-3034_959-3032delinsCAT	NP_001316079.1:n.959-3034_959-3032delinsCAT
NM_001329964.2:c.1740+290_1740+292delinsCAT	NP_001316893.1:n.1740+290_1740+292delinsCAT