Canonical Allele Identifier: CA16042467
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 373009
ClinVar RCV Id: RCV000414331
dbSNP Id: rs1057518137

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.189867892_189867894del , CM000665.2:g.189867892_189867894del GRCh38
NC_000003.11:g.189585681_189585683del , CM000665.1:g.189585681_189585683del GRCh37
NC_000003.10:g.191068375_191068377del NCBI36
NG_007550.1:g.241466_241468del
NG_007550.2:g.241466_241468del
NG_007550.3:g.276147_276149del

Transcript Alleles

HGVS Amino-acid change
ENST00000264731.8:c.942_944del MANE Select ENSP00000264731.3:p.Gly315del
ENST00000354600.10:c.660_662del MANE Plus Clinical ENSP00000346614.5:p.Gly221del
ENST00000264731.7:c.942_944del ENSP00000264731.3:p.Gly315del
ENST00000320472.9:c.942_944del ENSP00000317510.5:p.Gly315del
ENST00000354600.9:c.660_662del ENSP00000346614.5:p.Gly221del
ENST00000392460.7:c.942_944del ENSP00000376253.3:p.Gly315del
ENST00000392461.7:c.660_662del ENSP00000376254.3:p.Gly221del
ENST00000392463.6:c.660_662del ENSP00000376256.2:p.Gly221del
ENST00000418709.6:c.942_944del ENSP00000407144.2:p.Gly315del
ENST00000437221.5:c.660_662del ENSP00000392488.1:p.Gly221del
ENST00000440651.6:c.942_944del ENSP00000394337.2:p.Gly315del
ENST00000449992.5:c.405_407del ENSP00000387839.1:p.Gly136del
ENST00000456148.1:c.660_662del ENSP00000389485.1:p.Gly221del
ENST00000460036.1:n.766_768del
NM_001114978.1:c.942_944del NP_001108450.1:p.Gly315del
NM_001114979.1:c.942_944del NP_001108451.1:p.Gly315del
NM_001114980.1:c.660_662del NP_001108452.1:p.Gly221del
NM_001114981.1:c.660_662del NP_001108453.1:p.Gly221del
NM_001114982.1:c.660_662del NP_001108454.1:p.Gly221del
NM_003722.4:c.942_944del NP_003713.3:p.Gly315del
XM_005247843.2:c.942_944del XP_005247900.1:p.Gly315del
XM_005247844.3:c.891_893del XP_005247901.1:p.Gly298del
XM_005247846.2:c.942_944del XP_005247903.1:p.Gly315del
XM_011513251.1:c.939_941del XP_011511553.1:p.Gly314del
XM_011513252.1:c.936_938del XP_011511554.1:p.Gly313del
XM_011513253.1:c.903_905del XP_011511555.1:p.Gly302del
NM_001329144.1:c.942_944del NP_001316073.1:p.Gly315del
NM_001329145.1:c.660_662del NP_001316074.1:p.Gly221del
NM_001329146.1:c.405_407del NP_001316075.1:p.Gly136del
NM_001329148.1:c.942_944del NP_001316077.1:p.Gly315del
NM_001329149.1:c.660_662del NP_001316078.1:p.Gly221del
NM_001329150.1:c.405_407del NP_001316079.1:p.Gly136del
NM_001329964.1:c.936_938del NP_001316893.1:p.Gly313del
NM_003722.5:c.942_944del MANE Select NP_003713.3:p.Gly315del
NM_001114978.2:c.942_944del NP_001108450.1:p.Gly315del
NM_001114979.2:c.942_944del NP_001108451.1:p.Gly315del
NM_001114980.2:c.660_662del MANE Plus Clinical NP_001108452.1:p.Gly221del
NM_001114981.2:c.660_662del NP_001108453.1:p.Gly221del
NM_001114982.2:c.660_662del NP_001108454.1:p.Gly221del
NM_001329144.2:c.942_944del NP_001316073.1:p.Gly315del
NM_001329145.2:c.660_662del NP_001316074.1:p.Gly221del
NM_001329146.2:c.405_407del NP_001316075.1:p.Gly136del
NM_001329148.2:c.942_944del NP_001316077.1:p.Gly315del
NM_001329149.2:c.660_662del NP_001316078.1:p.Gly221del
NM_001329150.2:c.405_407del NP_001316079.1:p.Gly136del
NM_001329964.2:c.936_938del NP_001316893.1:p.Gly313del