Canonical Allele Identifier: CA1428533861

Gene: TP63

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189891241_189891242delinsAG , CM000665.2:g.189891241_189891242delinsAG	GRCh38
NC_000003.11:g.189609030_189609031delinsAG , CM000665.1:g.189609030_189609031delinsAG	GRCh37
NC_000003.10:g.191091724_191091725delinsAG	NCBI36
NG_007550.1:g.264815_264816delinsAG
NG_007550.2:g.264815_264816delinsAG
NG_007550.3:g.299496_299497delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264731.8:c.1746+359_1746+360delinsAG MANE Select	ENSP00000264731.3:n.1746+359_1746+360delinsAG
ENST00000354600.10:c.1464+359_1464+360delinsAG MANE Plus Clinical	ENSP00000346614.5:n.1464+359_1464+360delinsAG
ENST00000264731.7:c.1746+359_1746+360delinsAG	ENSP00000264731.3:n.1746+359_1746+360delinsAG
ENST00000320472.9:c.1508-2965_1508-2964delinsAG	ENSP00000317510.5:n.1508-2965_1508-2964delinsAG
ENST00000354600.9:c.1464+359_1464+360delinsAG	ENSP00000346614.5:n.1464+359_1464+360delinsAG
ENST00000392460.7:c.1652+1757_1652+1758delinsAG	ENSP00000376253.3:n.1652+1757_1652+1758delinsAG
ENST00000392461.7:c.1226-2965_1226-2964delinsAG	ENSP00000376254.3:n.1226-2965_1226-2964delinsAG
ENST00000392463.6:c.1370+1757_1370+1758delinsAG	ENSP00000376256.2:n.1370+1757_1370+1758delinsAG
ENST00000440651.6:c.1734+359_1734+360delinsAG	ENSP00000394337.2:n.1734+359_1734+360delinsAG
ENST00000449992.5:c.1209+359_1209+360delinsAG	ENSP00000387839.1:n.1209+359_1209+360delinsAG
ENST00000456148.1:c.1452+359_1452+360delinsAG	ENSP00000389485.1:n.1452+359_1452+360delinsAG
NM_001114978.1:c.1652+1757_1652+1758delinsAG	NP_001108450.1:n.1652+1757_1652+1758delinsAG
NM_001114980.1:c.1464+359_1464+360delinsAG	NP_001108452.1:n.1464+359_1464+360delinsAG
NM_001114981.1:c.1370+1757_1370+1758delinsAG	NP_001108453.1:n.1370+1757_1370+1758delinsAG
NM_003722.4:c.1746+359_1746+360delinsAG	NP_003713.3:n.1746+359_1746+360delinsAG
XM_005247843.2:c.1734+359_1734+360delinsAG	XP_005247900.1:n.1734+359_1734+360delinsAG
XM_005247844.3:c.1695+359_1695+360delinsAG	XP_005247901.1:n.1695+359_1695+360delinsAG
XM_011513251.1:c.1743+359_1743+360delinsAG	XP_011511553.1:n.1743+359_1743+360delinsAG
XM_011513252.1:c.1740+359_1740+360delinsAG	XP_011511554.1:n.1740+359_1740+360delinsAG
XM_011513253.1:c.1707+359_1707+360delinsAG	XP_011511555.1:n.1707+359_1707+360delinsAG
NM_001329144.1:c.1508-2965_1508-2964delinsAG	NP_001316073.1:n.1508-2965_1508-2964delinsAG
NM_001329145.1:c.1226-2965_1226-2964delinsAG	NP_001316074.1:n.1226-2965_1226-2964delinsAG
NM_001329146.1:c.1209+359_1209+360delinsAG	NP_001316075.1:n.1209+359_1209+360delinsAG
NM_001329148.1:c.1734+359_1734+360delinsAG	NP_001316077.1:n.1734+359_1734+360delinsAG
NM_001329149.1:c.1214-2965_1214-2964delinsAG	NP_001316078.1:n.1214-2965_1214-2964delinsAG
NM_001329150.1:c.959-2965_959-2964delinsAG	NP_001316079.1:n.959-2965_959-2964delinsAG
NM_001329964.1:c.1740+359_1740+360delinsAG	NP_001316893.1:n.1740+359_1740+360delinsAG
NM_003722.5:c.1746+359_1746+360delinsAG MANE Select	NP_003713.3:n.1746+359_1746+360delinsAG
NM_001114978.2:c.1652+1757_1652+1758delinsAG	NP_001108450.1:n.1652+1757_1652+1758delinsAG
NM_001114980.2:c.1464+359_1464+360delinsAG MANE Plus Clinical	NP_001108452.1:n.1464+359_1464+360delinsAG
NM_001114981.2:c.1370+1757_1370+1758delinsAG	NP_001108453.1:n.1370+1757_1370+1758delinsAG
NM_001329144.2:c.1508-2965_1508-2964delinsAG	NP_001316073.1:n.1508-2965_1508-2964delinsAG
NM_001329145.2:c.1226-2965_1226-2964delinsAG	NP_001316074.1:n.1226-2965_1226-2964delinsAG
NM_001329146.2:c.1209+359_1209+360delinsAG	NP_001316075.1:n.1209+359_1209+360delinsAG
NM_001329148.2:c.1734+359_1734+360delinsAG	NP_001316077.1:n.1734+359_1734+360delinsAG
NM_001329149.2:c.1214-2965_1214-2964delinsAG	NP_001316078.1:n.1214-2965_1214-2964delinsAG
NM_001329150.2:c.959-2965_959-2964delinsAG	NP_001316079.1:n.959-2965_959-2964delinsAG
NM_001329964.2:c.1740+359_1740+360delinsAG	NP_001316893.1:n.1740+359_1740+360delinsAG