Canonical Allele Identifier: CA355859296

Gene: TP63

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189738740G>C , CM000665.2:g.189738740G>C	GRCh38
NC_000003.11:g.189456529G>C , CM000665.1:g.189456529G>C	GRCh37
NC_000003.10:g.190939223G>C	NCBI36
NG_007550.1:g.112314G>C
NG_007550.2:g.112314G>C
NG_007550.3:g.146995G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_003722.5:c.290G>C MANE Select	NP_003713.3:p.Arg97Pro
ENST00000264731.8:c.290G>C MANE Select	ENSP00000264731.3:p.Arg97Pro
NM_001114978.1:c.290G>C	NP_001108450.1:p.Arg97Pro
NM_001114978.2:c.290G>C	NP_001108450.1:p.Arg97Pro
NM_001114979.1:c.290G>C	NP_001108451.1:p.Arg97Pro
NM_001114979.2:c.290G>C	NP_001108451.1:p.Arg97Pro
NM_001329144.1:c.290G>C	NP_001316073.1:p.Arg97Pro
NM_001329144.2:c.290G>C	NP_001316073.1:p.Arg97Pro
NM_001329148.1:c.290G>C	NP_001316077.1:p.Arg97Pro
NM_001329148.2:c.290G>C	NP_001316077.1:p.Arg97Pro
NM_001329964.1:c.284G>C	NP_001316893.1:p.Arg95Pro
NM_001329964.2:c.284G>C	NP_001316893.1:p.Arg95Pro
NM_003722.4:c.290G>C	NP_003713.3:p.Arg97Pro
ENST00000264731.7:c.290G>C	ENSP00000264731.3:p.Arg97Pro
ENST00000320472.9:c.290G>C	ENSP00000317510.5:p.Arg97Pro
ENST00000392460.7:c.290G>C	ENSP00000376253.3:p.Arg97Pro
ENST00000418709.6:c.290G>C	ENSP00000407144.2:p.Arg97Pro
ENST00000440651.6:c.290G>C	ENSP00000394337.2:p.Arg97Pro
ENST00000486398.1:n.390G>C
XM_005247843.2:c.290G>C	XP_005247900.1:p.Arg97Pro
XM_005247844.3:c.239G>C	XP_005247901.1:p.Arg80Pro
XM_005247846.2:c.290G>C	XP_005247903.1:p.Arg97Pro
XM_011513251.1:c.287G>C	XP_011511553.1:p.Arg96Pro
XM_011513252.1:c.284G>C	XP_011511554.1:p.Arg95Pro
XM_011513253.1:c.251G>C	XP_011511555.1:p.Arg84Pro