Canonical Allele Identifier: CA2752489

Gene: TP63

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189886509G>A , CM000665.2:g.189886509G>A	GRCh38
NC_000003.11:g.189604298G>A , CM000665.1:g.189604298G>A	GRCh37
NC_000003.10:g.191086992G>A	NCBI36
NG_007550.1:g.260083G>A
NG_007550.2:g.260083G>A
NG_007550.3:g.294764G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003722.5:c.1465G>A MANE Select	NP_003713.3:p.Ala489Thr
ENST00000264731.8:c.1465G>A MANE Select	ENSP00000264731.3:p.Ala489Thr
NM_001114980.2:c.1183G>A MANE Plus Clinical	NP_001108452.1:p.Ala395Thr
ENST00000354600.10:c.1183G>A MANE Plus Clinical	ENSP00000346614.5:p.Ala395Thr
NM_001114978.1:c.1465G>A	NP_001108450.1:p.Ala489Thr
NM_001114978.2:c.1465G>A	NP_001108450.1:p.Ala489Thr
NM_001114980.1:c.1183G>A	NP_001108452.1:p.Ala395Thr
NM_001114981.1:c.1183G>A	NP_001108453.1:p.Ala395Thr
NM_001114981.2:c.1183G>A	NP_001108453.1:p.Ala395Thr
NM_001329144.1:c.1465G>A	NP_001316073.1:p.Ala489Thr
NM_001329144.2:c.1465G>A	NP_001316073.1:p.Ala489Thr
NM_001329145.1:c.1183G>A	NP_001316074.1:p.Ala395Thr
NM_001329145.2:c.1183G>A	NP_001316074.1:p.Ala395Thr
NM_001329146.1:c.928G>A	NP_001316075.1:p.Ala310Thr
NM_001329146.2:c.928G>A	NP_001316075.1:p.Ala310Thr
NM_001329148.1:c.1453G>A	NP_001316077.1:p.Ala485Thr
NM_001329148.2:c.1453G>A	NP_001316077.1:p.Ala485Thr
NM_001329149.1:c.1171G>A	NP_001316078.1:p.Ala391Thr
NM_001329149.2:c.1171G>A	NP_001316078.1:p.Ala391Thr
NM_001329150.1:c.916G>A	NP_001316079.1:p.Ala306Thr
NM_001329150.2:c.916G>A	NP_001316079.1:p.Ala306Thr
NM_001329964.1:c.1459G>A	NP_001316893.1:p.Ala487Thr
NM_001329964.2:c.1459G>A	NP_001316893.1:p.Ala487Thr
NM_003722.4:c.1465G>A	NP_003713.3:p.Ala489Thr
ENST00000264731.7:c.1465G>A	ENSP00000264731.3:p.Ala489Thr
ENST00000320472.9:c.1465G>A	ENSP00000317510.5:p.Ala489Thr
ENST00000354600.9:c.1183G>A	ENSP00000346614.5:p.Ala395Thr
ENST00000392460.7:c.1465G>A	ENSP00000376253.3:p.Ala489Thr
ENST00000392461.7:c.1183G>A	ENSP00000376254.3:p.Ala395Thr
ENST00000392463.6:c.1183G>A	ENSP00000376256.2:p.Ala395Thr
ENST00000440651.6:c.1453G>A	ENSP00000394337.2:p.Ala485Thr
ENST00000449992.5:c.928G>A	ENSP00000387839.1:p.Ala310Thr
ENST00000456148.1:c.1171G>A	ENSP00000389485.1:p.Ala391Thr
XM_005247843.2:c.1453G>A	XP_005247900.1:p.Ala485Thr
XM_005247844.3:c.1414G>A	XP_005247901.1:p.Ala472Thr
XM_011513251.1:c.1462G>A	XP_011511553.1:p.Ala488Thr
XM_011513252.1:c.1459G>A	XP_011511554.1:p.Ala487Thr
XM_011513253.1:c.1426G>A	XP_011511555.1:p.Ala476Thr