Canonical Allele Identifier: CA2752065

Gene: TP63

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189738705G>A , CM000665.2:g.189738705G>A	GRCh38
NC_000003.11:g.189456494G>A , CM000665.1:g.189456494G>A	GRCh37
NC_000003.10:g.190939188G>A	NCBI36
NG_007550.1:g.112279G>A
NG_007550.2:g.112279G>A
NG_007550.3:g.146960G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264731.8:c.255G>A MANE Select	ENSP00000264731.3:p.Ala85=
ENST00000264731.7:c.255G>A	ENSP00000264731.3:p.Ala85=
ENST00000320472.9:c.255G>A	ENSP00000317510.5:p.Ala85=
ENST00000392460.7:c.255G>A	ENSP00000376253.3:p.Ala85=
ENST00000418709.6:c.255G>A	ENSP00000407144.2:p.Ala85=
ENST00000440651.6:c.255G>A	ENSP00000394337.2:p.Ala85=
ENST00000486398.1:n.355G>A
NM_001114978.1:c.255G>A	NP_001108450.1:p.Ala85=
NM_001114979.1:c.255G>A	NP_001108451.1:p.Ala85=
NM_003722.4:c.255G>A	NP_003713.3:p.Ala85=
XM_005247843.2:c.255G>A	XP_005247900.1:p.Ala85=
XM_005247844.3:c.204G>A	XP_005247901.1:p.Ala68=
XM_005247846.2:c.255G>A	XP_005247903.1:p.Ala85=
XM_011513251.1:c.252G>A	XP_011511553.1:p.Ala84=
XM_011513252.1:c.249G>A	XP_011511554.1:p.Ala83=
XM_011513253.1:c.216G>A	XP_011511555.1:p.Ala72=
NM_001329144.1:c.255G>A	NP_001316073.1:p.Ala85=
NM_001329148.1:c.255G>A	NP_001316077.1:p.Ala85=
NM_001329964.1:c.249G>A	NP_001316893.1:p.Ala83=
NM_003722.5:c.255G>A MANE Select	NP_003713.3:p.Ala85=
NM_001114978.2:c.255G>A	NP_001108450.1:p.Ala85=
NM_001114979.2:c.255G>A	NP_001108451.1:p.Ala85=
NM_001329144.2:c.255G>A	NP_001316073.1:p.Ala85=
NM_001329148.2:c.255G>A	NP_001316077.1:p.Ala85=
NM_001329964.2:c.249G>A	NP_001316893.1:p.Ala83=