Canonical Allele Identifier: CA1428419638

Gene: TP63

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189638424G= , CM000665.2:g.189638424G=	GRCh38
NC_000003.11:g.189356213G= , CM000665.1:g.189356213G=	GRCh37
NC_000003.10:g.190838907G=	NCBI36
NG_007550.1:g.11998G=
NG_007550.2:g.11998G=
NG_007550.3:g.46679G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264731.8:c.62+6847G= MANE Select	ENSP00000264731.3:n.62+6847G=
ENST00000264731.7:c.62+6847G=	ENSP00000264731.3:n.62+6847G=
ENST00000320472.9:c.62+6847G=	ENSP00000317510.5:n.62+6847G=
ENST00000392460.7:c.62+6847G=	ENSP00000376253.3:n.62+6847G=
ENST00000418709.6:c.62+6847G=	ENSP00000407144.2:n.62+6847G=
ENST00000440651.6:c.62+6847G=	ENSP00000394337.2:n.62+6847G=
ENST00000486398.1:n.162+6847G=
NM_001114978.1:c.62+6847G=	NP_001108450.1:n.62+6847G=
NM_001114979.1:c.62+6847G=	NP_001108451.1:n.62+6847G=
NM_003722.4:c.62+6847G=	NP_003713.3:n.62+6847G=
XM_005247843.2:c.62+6847G=	XP_005247900.1:n.62+6847G=
XM_005247844.3:c.11+7149G=	XP_005247901.1:n.11+7149G=
XM_005247846.2:c.62+6847G=	XP_005247903.1:n.62+6847G=
XM_011513251.1:c.59+15107G=	XP_011511553.1:n.59+15107G=
XM_011513252.1:c.56+41186G=	XP_011511554.1:n.56+41186G=
XM_011513253.1:c.23+71529G=	XP_011511555.1:n.23+71529G=
NM_001329144.1:c.62+6847G=	NP_001316073.1:n.62+6847G=
NM_001329148.1:c.62+6847G=	NP_001316077.1:n.62+6847G=
NM_001329964.1:c.56+41186G=	NP_001316893.1:n.56+41186G=
NM_003722.5:c.62+6847G= MANE Select	NP_003713.3:n.62+6847G=
NM_001114978.2:c.62+6847G=	NP_001108450.1:n.62+6847G=
NM_001114979.2:c.62+6847G=	NP_001108451.1:n.62+6847G=
NM_001329144.2:c.62+6847G=	NP_001316073.1:n.62+6847G=
NM_001329148.2:c.62+6847G=	NP_001316077.1:n.62+6847G=
NM_001329964.2:c.56+41186G=	NP_001316893.1:n.56+41186G=