Canonical Allele Identifier: CA2752518

Gene: TP63

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189889363C>A , CM000665.2:g.189889363C>A	GRCh38
NC_000003.11:g.189607152C>A , CM000665.1:g.189607152C>A	GRCh37
NC_000003.10:g.191089846C>A	NCBI36
NG_007550.1:g.262937C>A
NG_007550.2:g.262937C>A
NG_007550.3:g.297618C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003722.5:c.1531C>A MANE Select	NP_003713.3:p.Pro511Thr
ENST00000264731.8:c.1531C>A MANE Select	ENSP00000264731.3:p.Pro511Thr
NM_001114980.2:c.1249C>A MANE Plus Clinical	NP_001108452.1:p.Pro417Thr
ENST00000354600.10:c.1249C>A MANE Plus Clinical	ENSP00000346614.5:p.Pro417Thr
NM_001114978.1:c.1531C>A	NP_001108450.1:p.Pro511Thr
NM_001114978.2:c.1531C>A	NP_001108450.1:p.Pro511Thr
NM_001114980.1:c.1249C>A	NP_001108452.1:p.Pro417Thr
NM_001114981.1:c.1249C>A	NP_001108453.1:p.Pro417Thr
NM_001114981.2:c.1249C>A	NP_001108453.1:p.Pro417Thr
NM_001329144.1:c.1507+2812C>A	NP_001316073.1:n.1507+2812C>A
NM_001329144.2:c.1507+2812C>A	NP_001316073.1:n.1507+2812C>A
NM_001329145.1:c.1225+2812C>A	NP_001316074.1:n.1225+2812C>A
NM_001329145.2:c.1225+2812C>A	NP_001316074.1:n.1225+2812C>A
NM_001329146.1:c.994C>A	NP_001316075.1:p.Pro332Thr
NM_001329146.2:c.994C>A	NP_001316075.1:p.Pro332Thr
NM_001329148.1:c.1519C>A	NP_001316077.1:p.Pro507Thr
NM_001329148.2:c.1519C>A	NP_001316077.1:p.Pro507Thr
NM_001329149.1:c.1213+2812C>A	NP_001316078.1:n.1213+2812C>A
NM_001329149.2:c.1213+2812C>A	NP_001316078.1:n.1213+2812C>A
NM_001329150.1:c.958+2812C>A	NP_001316079.1:n.958+2812C>A
NM_001329150.2:c.958+2812C>A	NP_001316079.1:n.958+2812C>A
NM_001329964.1:c.1525C>A	NP_001316893.1:p.Pro509Thr
NM_001329964.2:c.1525C>A	NP_001316893.1:p.Pro509Thr
NM_003722.4:c.1531C>A	NP_003713.3:p.Pro511Thr
ENST00000264731.7:c.1531C>A	ENSP00000264731.3:p.Pro511Thr
ENST00000320472.9:c.1507+2812C>A	ENSP00000317510.5:n.1507+2812C>A
ENST00000354600.9:c.1249C>A	ENSP00000346614.5:p.Pro417Thr
ENST00000392460.7:c.1531C>A	ENSP00000376253.3:p.Pro511Thr
ENST00000392461.7:c.1225+2812C>A	ENSP00000376254.3:n.1225+2812C>A
ENST00000392463.6:c.1249C>A	ENSP00000376256.2:p.Pro417Thr
ENST00000440651.6:c.1519C>A	ENSP00000394337.2:p.Pro507Thr
ENST00000449992.5:c.994C>A	ENSP00000387839.1:p.Pro332Thr
ENST00000456148.1:c.1237C>A	ENSP00000389485.1:p.Pro413Thr
XM_005247843.2:c.1519C>A	XP_005247900.1:p.Pro507Thr
XM_005247844.3:c.1480C>A	XP_005247901.1:p.Pro494Thr
XM_011513251.1:c.1528C>A	XP_011511553.1:p.Pro510Thr
XM_011513252.1:c.1525C>A	XP_011511554.1:p.Pro509Thr
XM_011513253.1:c.1492C>A	XP_011511555.1:p.Pro498Thr