Canonical Allele Identifier: CA355751104

Gene: TP63

Linked Data

• dbSNP Id: rs2108872899
• MyVariant Identifiers: chr3:g.189611998C>A (hg19) ; chr3:g.189894209C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189894209C>A , CM000665.2:g.189894209C>A	GRCh38
NC_000003.11:g.189611998C>A , CM000665.1:g.189611998C>A	GRCh37
NC_000003.10:g.191094692C>A	NCBI36
NG_007550.1:g.267783C>A
NG_007550.2:g.267783C>A
NG_007550.3:g.302464C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264731.8:c.1750C>A MANE Select	ENSP00000264731.3:p.Leu584Met
ENST00000354600.10:c.1468C>A MANE Plus Clinical	ENSP00000346614.5:p.Leu490Met
ENST00000264731.7:c.1750C>A	ENSP00000264731.3:p.Leu584Met
ENST00000320472.9:c.1511C>A	ENSP00000317510.5:p.Ser504Tyr
ENST00000354600.9:c.1468C>A	ENSP00000346614.5:p.Leu490Met
ENST00000392460.7:c.1656C>A	ENSP00000376253.3:p.Ile552=
ENST00000392461.7:c.1229C>A	ENSP00000376254.3:p.Ser410Tyr
ENST00000392463.6:c.1374C>A	ENSP00000376256.2:p.Ile458=
ENST00000440651.6:c.1738C>A	ENSP00000394337.2:p.Leu580Met
ENST00000449992.5:c.1213C>A	ENSP00000387839.1:p.Leu405Met
ENST00000456148.1:c.1456C>A	ENSP00000389485.1:p.Leu486Met
NM_001114978.1:c.1656C>A	NP_001108450.1:p.Ile552=
NM_001114980.1:c.1468C>A	NP_001108452.1:p.Leu490Met
NM_001114981.1:c.1374C>A	NP_001108453.1:p.Ile458=
NM_003722.4:c.1750C>A	NP_003713.3:p.Leu584Met
XM_005247843.2:c.1738C>A	XP_005247900.1:p.Leu580Met
XM_005247844.3:c.1699C>A	XP_005247901.1:p.Leu567Met
XM_011513251.1:c.1747C>A	XP_011511553.1:p.Leu583Met
XM_011513252.1:c.1744C>A	XP_011511554.1:p.Leu582Met
XM_011513253.1:c.1711C>A	XP_011511555.1:p.Leu571Met
NM_001329144.1:c.1511C>A	NP_001316073.1:p.Ser504Tyr
NM_001329145.1:c.1229C>A	NP_001316074.1:p.Ser410Tyr
NM_001329146.1:c.1213C>A	NP_001316075.1:p.Leu405Met
NM_001329148.1:c.1738C>A	NP_001316077.1:p.Leu580Met
NM_001329149.1:c.1217C>A	NP_001316078.1:p.Ser406Tyr
NM_001329150.1:c.962C>A	NP_001316079.1:p.Ser321Tyr
NM_001329964.1:c.1744C>A	NP_001316893.1:p.Leu582Met
NM_003722.5:c.1750C>A MANE Select	NP_003713.3:p.Leu584Met
NM_001114978.2:c.1656C>A	NP_001108450.1:p.Ile552=
NM_001114980.2:c.1468C>A MANE Plus Clinical	NP_001108452.1:p.Leu490Met
NM_001114981.2:c.1374C>A	NP_001108453.1:p.Ile458=
NM_001329144.2:c.1511C>A	NP_001316073.1:p.Ser504Tyr
NM_001329145.2:c.1229C>A	NP_001316074.1:p.Ser410Tyr
NM_001329146.2:c.1213C>A	NP_001316075.1:p.Leu405Met
NM_001329148.2:c.1738C>A	NP_001316077.1:p.Leu580Met
NM_001329149.2:c.1217C>A	NP_001316078.1:p.Ser406Tyr
NM_001329150.2:c.962C>A	NP_001316079.1:p.Ser321Tyr
NM_001329964.2:c.1744C>A	NP_001316893.1:p.Leu582Met