Canonical Allele Identifier: CA1428533789

Gene: TP63

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189891090_189891095delinsGCTTGT , CM000665.2:g.189891090_189891095delinsGCTTGT	GRCh38
NC_000003.11:g.189608879_189608884delinsGCTTGT , CM000665.1:g.189608879_189608884delinsGCTTGT	GRCh37
NC_000003.10:g.191091573_191091578delinsGCTTGT	NCBI36
NG_007550.1:g.264664_264669delinsGCTTGT
NG_007550.2:g.264664_264669delinsGCTTGT
NG_007550.3:g.299345_299350delinsGCTTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264731.8:c.1746+208_1746+213delinsGCTTGT MANE Select	ENSP00000264731.3:n.1746+208_1746+213delinsGCTTGT
ENST00000354600.10:c.1464+208_1464+213delinsGCTTGT MANE Plus Clinical	ENSP00000346614.5:n.1464+208_1464+213delinsGCTTGT
ENST00000264731.7:c.1746+208_1746+213delinsGCTTGT	ENSP00000264731.3:n.1746+208_1746+213delinsGCTTGT
ENST00000320472.9:c.1508-3116_1508-3111delinsGCTTGT	ENSP00000317510.5:n.1508-3116_1508-3111delinsGCTTGT
ENST00000354600.9:c.1464+208_1464+213delinsGCTTGT	ENSP00000346614.5:n.1464+208_1464+213delinsGCTTGT
ENST00000392460.7:c.1652+1606_1652+1611delinsGCTTGT	ENSP00000376253.3:n.1652+1606_1652+1611delinsGCTTGT
ENST00000392461.7:c.1226-3116_1226-3111delinsGCTTGT	ENSP00000376254.3:n.1226-3116_1226-3111delinsGCTTGT
ENST00000392463.6:c.1370+1606_1370+1611delinsGCTTGT	ENSP00000376256.2:n.1370+1606_1370+1611delinsGCTTGT
ENST00000440651.6:c.1734+208_1734+213delinsGCTTGT	ENSP00000394337.2:n.1734+208_1734+213delinsGCTTGT
ENST00000449992.5:c.1209+208_1209+213delinsGCTTGT	ENSP00000387839.1:n.1209+208_1209+213delinsGCTTGT
ENST00000456148.1:c.1452+208_1452+213delinsGCTTGT	ENSP00000389485.1:n.1452+208_1452+213delinsGCTTGT
NM_001114978.1:c.1652+1606_1652+1611delinsGCTTGT	NP_001108450.1:n.1652+1606_1652+1611delinsGCTTGT
NM_001114980.1:c.1464+208_1464+213delinsGCTTGT	NP_001108452.1:n.1464+208_1464+213delinsGCTTGT
NM_001114981.1:c.1370+1606_1370+1611delinsGCTTGT	NP_001108453.1:n.1370+1606_1370+1611delinsGCTTGT
NM_003722.4:c.1746+208_1746+213delinsGCTTGT	NP_003713.3:n.1746+208_1746+213delinsGCTTGT
XM_005247843.2:c.1734+208_1734+213delinsGCTTGT	XP_005247900.1:n.1734+208_1734+213delinsGCTTGT
XM_005247844.3:c.1695+208_1695+213delinsGCTTGT	XP_005247901.1:n.1695+208_1695+213delinsGCTTGT
XM_011513251.1:c.1743+208_1743+213delinsGCTTGT	XP_011511553.1:n.1743+208_1743+213delinsGCTTGT
XM_011513252.1:c.1740+208_1740+213delinsGCTTGT	XP_011511554.1:n.1740+208_1740+213delinsGCTTGT
XM_011513253.1:c.1707+208_1707+213delinsGCTTGT	XP_011511555.1:n.1707+208_1707+213delinsGCTTGT
NM_001329144.1:c.1508-3116_1508-3111delinsGCTTGT	NP_001316073.1:n.1508-3116_1508-3111delinsGCTTGT
NM_001329145.1:c.1226-3116_1226-3111delinsGCTTGT	NP_001316074.1:n.1226-3116_1226-3111delinsGCTTGT
NM_001329146.1:c.1209+208_1209+213delinsGCTTGT	NP_001316075.1:n.1209+208_1209+213delinsGCTTGT
NM_001329148.1:c.1734+208_1734+213delinsGCTTGT	NP_001316077.1:n.1734+208_1734+213delinsGCTTGT
NM_001329149.1:c.1214-3116_1214-3111delinsGCTTGT	NP_001316078.1:n.1214-3116_1214-3111delinsGCTTGT
NM_001329150.1:c.959-3116_959-3111delinsGCTTGT	NP_001316079.1:n.959-3116_959-3111delinsGCTTGT
NM_001329964.1:c.1740+208_1740+213delinsGCTTGT	NP_001316893.1:n.1740+208_1740+213delinsGCTTGT
NM_003722.5:c.1746+208_1746+213delinsGCTTGT MANE Select	NP_003713.3:n.1746+208_1746+213delinsGCTTGT
NM_001114978.2:c.1652+1606_1652+1611delinsGCTTGT	NP_001108450.1:n.1652+1606_1652+1611delinsGCTTGT
NM_001114980.2:c.1464+208_1464+213delinsGCTTGT MANE Plus Clinical	NP_001108452.1:n.1464+208_1464+213delinsGCTTGT
NM_001114981.2:c.1370+1606_1370+1611delinsGCTTGT	NP_001108453.1:n.1370+1606_1370+1611delinsGCTTGT
NM_001329144.2:c.1508-3116_1508-3111delinsGCTTGT	NP_001316073.1:n.1508-3116_1508-3111delinsGCTTGT
NM_001329145.2:c.1226-3116_1226-3111delinsGCTTGT	NP_001316074.1:n.1226-3116_1226-3111delinsGCTTGT
NM_001329146.2:c.1209+208_1209+213delinsGCTTGT	NP_001316075.1:n.1209+208_1209+213delinsGCTTGT
NM_001329148.2:c.1734+208_1734+213delinsGCTTGT	NP_001316077.1:n.1734+208_1734+213delinsGCTTGT
NM_001329149.2:c.1214-3116_1214-3111delinsGCTTGT	NP_001316078.1:n.1214-3116_1214-3111delinsGCTTGT
NM_001329150.2:c.959-3116_959-3111delinsGCTTGT	NP_001316079.1:n.959-3116_959-3111delinsGCTTGT
NM_001329964.2:c.1740+208_1740+213delinsGCTTGT	NP_001316893.1:n.1740+208_1740+213delinsGCTTGT