Canonical Allele Identifier: CA2759859948

Gene: TP63

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189891198_189891202dup , CM000665.2:g.189891198_189891202dup	GRCh38
NC_000003.11:g.189608987_189608991dup , CM000665.1:g.189608987_189608991dup	GRCh37
NC_000003.10:g.191091681_191091685dup	NCBI36
NG_007550.1:g.264772_264776dup
NG_007550.2:g.264772_264776dup
NG_007550.3:g.299453_299457dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264731.8:c.1746+316_1746+320dup MANE Select	ENSP00000264731.3:n.1746+316_1746+320dup
ENST00000354600.10:c.1464+316_1464+320dup MANE Plus Clinical	ENSP00000346614.5:n.1464+316_1464+320dup
ENST00000264731.7:c.1746+316_1746+320dup	ENSP00000264731.3:n.1746+316_1746+320dup
ENST00000320472.9:c.1508-3008_1508-3004dup	ENSP00000317510.5:n.1508-3008_1508-3004dup
ENST00000354600.9:c.1464+316_1464+320dup	ENSP00000346614.5:n.1464+316_1464+320dup
ENST00000392460.7:c.1652+1714_1652+1718dup	ENSP00000376253.3:n.1652+1714_1652+1718dup
ENST00000392461.7:c.1226-3008_1226-3004dup	ENSP00000376254.3:n.1226-3008_1226-3004dup
ENST00000392463.6:c.1370+1714_1370+1718dup	ENSP00000376256.2:n.1370+1714_1370+1718dup
ENST00000440651.6:c.1734+316_1734+320dup	ENSP00000394337.2:n.1734+316_1734+320dup
ENST00000449992.5:c.1209+316_1209+320dup	ENSP00000387839.1:n.1209+316_1209+320dup
ENST00000456148.1:c.1452+316_1452+320dup	ENSP00000389485.1:n.1452+316_1452+320dup
NM_001114978.1:c.1652+1714_1652+1718dup	NP_001108450.1:n.1652+1714_1652+1718dup
NM_001114980.1:c.1464+316_1464+320dup	NP_001108452.1:n.1464+316_1464+320dup
NM_001114981.1:c.1370+1714_1370+1718dup	NP_001108453.1:n.1370+1714_1370+1718dup
NM_003722.4:c.1746+316_1746+320dup	NP_003713.3:n.1746+316_1746+320dup
XM_005247843.2:c.1734+316_1734+320dup	XP_005247900.1:n.1734+316_1734+320dup
XM_005247844.3:c.1695+316_1695+320dup	XP_005247901.1:n.1695+316_1695+320dup
XM_011513251.1:c.1743+316_1743+320dup	XP_011511553.1:n.1743+316_1743+320dup
XM_011513252.1:c.1740+316_1740+320dup	XP_011511554.1:n.1740+316_1740+320dup
XM_011513253.1:c.1707+316_1707+320dup	XP_011511555.1:n.1707+316_1707+320dup
NM_001329144.1:c.1508-3008_1508-3004dup	NP_001316073.1:n.1508-3008_1508-3004dup
NM_001329145.1:c.1226-3008_1226-3004dup	NP_001316074.1:n.1226-3008_1226-3004dup
NM_001329146.1:c.1209+316_1209+320dup	NP_001316075.1:n.1209+316_1209+320dup
NM_001329148.1:c.1734+316_1734+320dup	NP_001316077.1:n.1734+316_1734+320dup
NM_001329149.1:c.1214-3008_1214-3004dup	NP_001316078.1:n.1214-3008_1214-3004dup
NM_001329150.1:c.959-3008_959-3004dup	NP_001316079.1:n.959-3008_959-3004dup
NM_001329964.1:c.1740+316_1740+320dup	NP_001316893.1:n.1740+316_1740+320dup
NM_003722.5:c.1746+316_1746+320dup MANE Select	NP_003713.3:n.1746+316_1746+320dup
NM_001114978.2:c.1652+1714_1652+1718dup	NP_001108450.1:n.1652+1714_1652+1718dup
NM_001114980.2:c.1464+316_1464+320dup MANE Plus Clinical	NP_001108452.1:n.1464+316_1464+320dup
NM_001114981.2:c.1370+1714_1370+1718dup	NP_001108453.1:n.1370+1714_1370+1718dup
NM_001329144.2:c.1508-3008_1508-3004dup	NP_001316073.1:n.1508-3008_1508-3004dup
NM_001329145.2:c.1226-3008_1226-3004dup	NP_001316074.1:n.1226-3008_1226-3004dup
NM_001329146.2:c.1209+316_1209+320dup	NP_001316075.1:n.1209+316_1209+320dup
NM_001329148.2:c.1734+316_1734+320dup	NP_001316077.1:n.1734+316_1734+320dup
NM_001329149.2:c.1214-3008_1214-3004dup	NP_001316078.1:n.1214-3008_1214-3004dup
NM_001329150.2:c.959-3008_959-3004dup	NP_001316079.1:n.959-3008_959-3004dup
NM_001329964.2:c.1740+316_1740+320dup	NP_001316893.1:n.1740+316_1740+320dup