Canonical Allele Identifier: CA355751133

Gene: TP63

Linked Data

• dbSNP Id: rs2108872965
• MyVariant Identifiers: chr3:g.189612007C>G (hg19) ; chr3:g.189894218C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189894218C>G , CM000665.2:g.189894218C>G	GRCh38
NC_000003.11:g.189612007C>G , CM000665.1:g.189612007C>G	GRCh37
NC_000003.10:g.191094701C>G	NCBI36
NG_007550.1:g.267792C>G
NG_007550.2:g.267792C>G
NG_007550.3:g.302473C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264731.8:c.1759C>G MANE Select	ENSP00000264731.3:p.Leu587Val
ENST00000354600.10:c.1477C>G MANE Plus Clinical	ENSP00000346614.5:p.Leu493Val
ENST00000264731.7:c.1759C>G	ENSP00000264731.3:p.Leu587Val
ENST00000320472.9:c.1520C>G	ENSP00000317510.5:p.Ser507Cys
ENST00000354600.9:c.1477C>G	ENSP00000346614.5:p.Leu493Val
ENST00000392460.7:c.1665C>G	ENSP00000376253.3:p.Val555=
ENST00000392461.7:c.1238C>G	ENSP00000376254.3:p.Ser413Cys
ENST00000392463.6:c.1383C>G	ENSP00000376256.2:p.Val461=
ENST00000440651.6:c.1747C>G	ENSP00000394337.2:p.Leu583Val
ENST00000449992.5:c.1222C>G	ENSP00000387839.1:p.Leu408Val
ENST00000456148.1:c.1465C>G	ENSP00000389485.1:p.Leu489Val
NM_001114978.1:c.1665C>G	NP_001108450.1:p.Val555=
NM_001114980.1:c.1477C>G	NP_001108452.1:p.Leu493Val
NM_001114981.1:c.1383C>G	NP_001108453.1:p.Val461=
NM_003722.4:c.1759C>G	NP_003713.3:p.Leu587Val
XM_005247843.2:c.1747C>G	XP_005247900.1:p.Leu583Val
XM_005247844.3:c.1708C>G	XP_005247901.1:p.Leu570Val
XM_011513251.1:c.1756C>G	XP_011511553.1:p.Leu586Val
XM_011513252.1:c.1753C>G	XP_011511554.1:p.Leu585Val
XM_011513253.1:c.1720C>G	XP_011511555.1:p.Leu574Val
NM_001329144.1:c.1520C>G	NP_001316073.1:p.Ser507Cys
NM_001329145.1:c.1238C>G	NP_001316074.1:p.Ser413Cys
NM_001329146.1:c.1222C>G	NP_001316075.1:p.Leu408Val
NM_001329148.1:c.1747C>G	NP_001316077.1:p.Leu583Val
NM_001329149.1:c.1226C>G	NP_001316078.1:p.Ser409Cys
NM_001329150.1:c.971C>G	NP_001316079.1:p.Ser324Cys
NM_001329964.1:c.1753C>G	NP_001316893.1:p.Leu585Val
NM_003722.5:c.1759C>G MANE Select	NP_003713.3:p.Leu587Val
NM_001114978.2:c.1665C>G	NP_001108450.1:p.Val555=
NM_001114980.2:c.1477C>G MANE Plus Clinical	NP_001108452.1:p.Leu493Val
NM_001114981.2:c.1383C>G	NP_001108453.1:p.Val461=
NM_001329144.2:c.1520C>G	NP_001316073.1:p.Ser507Cys
NM_001329145.2:c.1238C>G	NP_001316074.1:p.Ser413Cys
NM_001329146.2:c.1222C>G	NP_001316075.1:p.Leu408Val
NM_001329148.2:c.1747C>G	NP_001316077.1:p.Leu583Val
NM_001329149.2:c.1226C>G	NP_001316078.1:p.Ser409Cys
NM_001329150.2:c.971C>G	NP_001316079.1:p.Ser324Cys
NM_001329964.2:c.1753C>G	NP_001316893.1:p.Leu585Val