Canonical Allele Identifier: CA2752480

Gene: TP63

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189886448A>G , CM000665.2:g.189886448A>G	GRCh38
NC_000003.11:g.189604237A>G , CM000665.1:g.189604237A>G	GRCh37
NC_000003.10:g.191086931A>G	NCBI36
NG_007550.1:g.260022A>G
NG_007550.2:g.260022A>G
NG_007550.3:g.294703A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_003722.5:c.1404A>G MANE Select	NP_003713.3:p.Lys468=
ENST00000264731.8:c.1404A>G MANE Select	ENSP00000264731.3:p.Lys468=
NM_001114980.2:c.1122A>G MANE Plus Clinical	NP_001108452.1:p.Lys374=
ENST00000354600.10:c.1122A>G MANE Plus Clinical	ENSP00000346614.5:p.Lys374=
NM_001114978.1:c.1404A>G	NP_001108450.1:p.Lys468=
NM_001114978.2:c.1404A>G	NP_001108450.1:p.Lys468=
NM_001114980.1:c.1122A>G	NP_001108452.1:p.Lys374=
NM_001114981.1:c.1122A>G	NP_001108453.1:p.Lys374=
NM_001114981.2:c.1122A>G	NP_001108453.1:p.Lys374=
NM_001329144.1:c.1404A>G	NP_001316073.1:p.Lys468=
NM_001329144.2:c.1404A>G	NP_001316073.1:p.Lys468=
NM_001329145.1:c.1122A>G	NP_001316074.1:p.Lys374=
NM_001329145.2:c.1122A>G	NP_001316074.1:p.Lys374=
NM_001329146.1:c.867A>G	NP_001316075.1:p.Lys289=
NM_001329146.2:c.867A>G	NP_001316075.1:p.Lys289=
NM_001329148.1:c.1392A>G	NP_001316077.1:p.Lys464=
NM_001329148.2:c.1392A>G	NP_001316077.1:p.Lys464=
NM_001329149.1:c.1110A>G	NP_001316078.1:p.Lys370=
NM_001329149.2:c.1110A>G	NP_001316078.1:p.Lys370=
NM_001329150.1:c.855A>G	NP_001316079.1:p.Lys285=
NM_001329150.2:c.855A>G	NP_001316079.1:p.Lys285=
NM_001329964.1:c.1398A>G	NP_001316893.1:p.Lys466=
NM_001329964.2:c.1398A>G	NP_001316893.1:p.Lys466=
NM_003722.4:c.1404A>G	NP_003713.3:p.Lys468=
ENST00000264731.7:c.1404A>G	ENSP00000264731.3:p.Lys468=
ENST00000320472.9:c.1404A>G	ENSP00000317510.5:p.Lys468=
ENST00000354600.9:c.1122A>G	ENSP00000346614.5:p.Lys374=
ENST00000392460.7:c.1404A>G	ENSP00000376253.3:p.Lys468=
ENST00000392461.7:c.1122A>G	ENSP00000376254.3:p.Lys374=
ENST00000392463.6:c.1122A>G	ENSP00000376256.2:p.Lys374=
ENST00000440651.6:c.1392A>G	ENSP00000394337.2:p.Lys464=
ENST00000449992.5:c.867A>G	ENSP00000387839.1:p.Lys289=
ENST00000456148.1:c.1110A>G	ENSP00000389485.1:p.Lys370=
XM_005247843.2:c.1392A>G	XP_005247900.1:p.Lys464=
XM_005247844.3:c.1353A>G	XP_005247901.1:p.Lys451=
XM_011513251.1:c.1401A>G	XP_011511553.1:p.Lys467=
XM_011513252.1:c.1398A>G	XP_011511554.1:p.Lys466=
XM_011513253.1:c.1365A>G	XP_011511555.1:p.Lys455=