Canonical Allele Identifier: CA1428496008

Gene: TP63

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189868708C= , CM000665.2:g.189868708C=	GRCh38
NC_000003.11:g.189586497C= , CM000665.1:g.189586497C=	GRCh37
NC_000003.10:g.191069191C=	NCBI36
NG_007550.1:g.242282C=
NG_007550.2:g.242282C=
NG_007550.3:g.276963C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264731.8:c.1121C= MANE Select	ENSP00000264731.3:p.Thr374=
ENST00000354600.10:c.839C= MANE Plus Clinical	ENSP00000346614.5:p.Thr280=
ENST00000264731.7:c.1121C=	ENSP00000264731.3:p.Thr374=
ENST00000320472.9:c.1121C=	ENSP00000317510.5:p.Thr374=
ENST00000354600.9:c.839C=	ENSP00000346614.5:p.Thr280=
ENST00000392460.7:c.1121C=	ENSP00000376253.3:p.Thr374=
ENST00000392461.7:c.839C=	ENSP00000376254.3:p.Thr280=
ENST00000392463.6:c.839C=	ENSP00000376256.2:p.Thr280=
ENST00000418709.6:c.1121C=	ENSP00000407144.2:p.Thr374=
ENST00000437221.5:c.839C=	ENSP00000392488.1:p.Thr280=
ENST00000440651.6:c.1117+4C=	ENSP00000394337.2:n.1117+4C=
ENST00000449992.5:c.584C=	ENSP00000387839.1:p.Thr195=
ENST00000456148.1:c.835+4C=	ENSP00000389485.1:n.835+4C=
ENST00000460036.1:n.945C=
NM_001114978.1:c.1121C=	NP_001108450.1:p.Thr374=
NM_001114979.1:c.1121C=	NP_001108451.1:p.Thr374=
NM_001114980.1:c.839C=	NP_001108452.1:p.Thr280=
NM_001114981.1:c.839C=	NP_001108453.1:p.Thr280=
NM_001114982.1:c.839C=	NP_001108454.1:p.Thr280=
NM_003722.4:c.1121C=	NP_003713.3:p.Thr374=
XM_005247843.2:c.1117+4C=	XP_005247900.1:n.1117+4C=
XM_005247844.3:c.1070C=	XP_005247901.1:p.Thr357=
XM_005247846.2:c.1117+4C=	XP_005247903.1:n.1117+4C=
XM_011513251.1:c.1118C=	XP_011511553.1:p.Thr373=
XM_011513252.1:c.1115C=	XP_011511554.1:p.Thr372=
XM_011513253.1:c.1082C=	XP_011511555.1:p.Thr361=
NM_001329144.1:c.1121C=	NP_001316073.1:p.Thr374=
NM_001329145.1:c.839C=	NP_001316074.1:p.Thr280=
NM_001329146.1:c.584C=	NP_001316075.1:p.Thr195=
NM_001329148.1:c.1117+4C=	NP_001316077.1:n.1117+4C=
NM_001329149.1:c.835+4C=	NP_001316078.1:n.835+4C=
NM_001329150.1:c.580+4C=	NP_001316079.1:n.580+4C=
NM_001329964.1:c.1115C=	NP_001316893.1:p.Thr372=
NM_003722.5:c.1121C= MANE Select	NP_003713.3:p.Thr374=
NM_001114978.2:c.1121C=	NP_001108450.1:p.Thr374=
NM_001114979.2:c.1121C=	NP_001108451.1:p.Thr374=
NM_001114980.2:c.839C= MANE Plus Clinical	NP_001108452.1:p.Thr280=
NM_001114981.2:c.839C=	NP_001108453.1:p.Thr280=
NM_001114982.2:c.839C=	NP_001108454.1:p.Thr280=
NM_001329144.2:c.1121C=	NP_001316073.1:p.Thr374=
NM_001329145.2:c.839C=	NP_001316074.1:p.Thr280=
NM_001329146.2:c.584C=	NP_001316075.1:p.Thr195=
NM_001329148.2:c.1117+4C=	NP_001316077.1:n.1117+4C=
NM_001329149.2:c.835+4C=	NP_001316078.1:n.835+4C=
NM_001329150.2:c.580+4C=	NP_001316079.1:n.580+4C=
NM_001329964.2:c.1115C=	NP_001316893.1:p.Thr372=