Canonical Allele Identifier: CA1428525448

Gene: TP63

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189864361G= , CM000665.2:g.189864361G=	GRCh38
NC_000003.11:g.189582150G= , CM000665.1:g.189582150G=	GRCh37
NC_000003.10:g.191064844G=	NCBI36
NG_007550.1:g.237935G=
NG_007550.2:g.237935G=
NG_007550.3:g.272616G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264731.8:c.709G= MANE Select	ENSP00000264731.3:p.Val237=
ENST00000354600.10:c.427G= MANE Plus Clinical	ENSP00000346614.5:p.Val143=
ENST00000264731.7:c.709G=	ENSP00000264731.3:p.Val237=
ENST00000320472.9:c.709G=	ENSP00000317510.5:p.Val237=
ENST00000354600.9:c.427G=	ENSP00000346614.5:p.Val143=
ENST00000392460.7:c.709G=	ENSP00000376253.3:p.Val237=
ENST00000392461.7:c.427G=	ENSP00000376254.3:p.Val143=
ENST00000392463.6:c.427G=	ENSP00000376256.2:p.Val143=
ENST00000418709.6:c.709G=	ENSP00000407144.2:p.Val237=
ENST00000437221.5:c.427G=	ENSP00000392488.1:p.Val143=
ENST00000440651.6:c.709G=	ENSP00000394337.2:p.Val237=
ENST00000449992.5:c.172G=	ENSP00000387839.1:p.Val58=
ENST00000456148.1:c.427G=	ENSP00000389485.1:p.Val143=
ENST00000460036.1:n.533G=
NM_001114978.1:c.709G=	NP_001108450.1:p.Val237=
NM_001114979.1:c.709G=	NP_001108451.1:p.Val237=
NM_001114980.1:c.427G=	NP_001108452.1:p.Val143=
NM_001114981.1:c.427G=	NP_001108453.1:p.Val143=
NM_001114982.1:c.427G=	NP_001108454.1:p.Val143=
NM_003722.4:c.709G=	NP_003713.3:p.Val237=
XM_005247843.2:c.709G=	XP_005247900.1:p.Val237=
XM_005247844.3:c.658G=	XP_005247901.1:p.Val220=
XM_005247846.2:c.709G=	XP_005247903.1:p.Val237=
XM_011513251.1:c.706G=	XP_011511553.1:p.Val236=
XM_011513252.1:c.703G=	XP_011511554.1:p.Val235=
XM_011513253.1:c.670G=	XP_011511555.1:p.Val224=
NM_001329144.1:c.709G=	NP_001316073.1:p.Val237=
NM_001329145.1:c.427G=	NP_001316074.1:p.Val143=
NM_001329146.1:c.172G=	NP_001316075.1:p.Val58=
NM_001329148.1:c.709G=	NP_001316077.1:p.Val237=
NM_001329149.1:c.427G=	NP_001316078.1:p.Val143=
NM_001329150.1:c.172G=	NP_001316079.1:p.Val58=
NM_001329964.1:c.703G=	NP_001316893.1:p.Val235=
NM_003722.5:c.709G= MANE Select	NP_003713.3:p.Val237=
NM_001114978.2:c.709G=	NP_001108450.1:p.Val237=
NM_001114979.2:c.709G=	NP_001108451.1:p.Val237=
NM_001114980.2:c.427G= MANE Plus Clinical	NP_001108452.1:p.Val143=
NM_001114981.2:c.427G=	NP_001108453.1:p.Val143=
NM_001114982.2:c.427G=	NP_001108454.1:p.Val143=
NM_001329144.2:c.709G=	NP_001316073.1:p.Val237=
NM_001329145.2:c.427G=	NP_001316074.1:p.Val143=
NM_001329146.2:c.172G=	NP_001316075.1:p.Val58=
NM_001329148.2:c.709G=	NP_001316077.1:p.Val237=
NM_001329149.2:c.427G=	NP_001316078.1:p.Val143=
NM_001329150.2:c.172G=	NP_001316079.1:p.Val58=
NM_001329964.2:c.703G=	NP_001316893.1:p.Val235=