Canonical Allele Identifier: CA16042432
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 372786
ClinVar RCV Id: RCV000414612
dbSNP Id: rs1057517984
MyVariant Identifiers: chr3:g.189582046A>G (hg19) chr3:g.189864257A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.189864257A>G , CM000665.2:g.189864257A>G GRCh38
NC_000003.11:g.189582046A>G , CM000665.1:g.189582046A>G GRCh37
NC_000003.10:g.191064740A>G NCBI36
NG_007550.1:g.237831A>G
NG_007550.2:g.237831A>G
NG_007550.3:g.272512A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264731.8:c.605A>G MANE Select ENSP00000264731.3:p.Tyr202Cys
ENST00000354600.10:c.323A>G MANE Plus Clinical ENSP00000346614.5:p.Tyr108Cys
ENST00000264731.7:c.605A>G ENSP00000264731.3:p.Tyr202Cys
ENST00000320472.9:c.605A>G ENSP00000317510.5:p.Tyr202Cys
ENST00000354600.9:c.323A>G ENSP00000346614.5:p.Tyr108Cys
ENST00000392460.7:c.605A>G ENSP00000376253.3:p.Tyr202Cys
ENST00000392461.7:c.323A>G ENSP00000376254.3:p.Tyr108Cys
ENST00000392463.6:c.323A>G ENSP00000376256.2:p.Tyr108Cys
ENST00000418709.6:c.605A>G ENSP00000407144.2:p.Tyr202Cys
ENST00000434928.5:c.539A>G ENSP00000401661.1:p.Tyr180Cys
ENST00000437221.5:c.323A>G ENSP00000392488.1:p.Tyr108Cys
ENST00000440651.6:c.605A>G ENSP00000394337.2:p.Tyr202Cys
ENST00000449992.5:c.68A>G ENSP00000387839.1:p.Tyr23Cys
ENST00000456148.1:c.323A>G ENSP00000389485.1:p.Tyr108Cys
ENST00000460036.1:n.429A>G
NM_001114978.1:c.605A>G NP_001108450.1:p.Tyr202Cys
NM_001114979.1:c.605A>G NP_001108451.1:p.Tyr202Cys
NM_001114980.1:c.323A>G NP_001108452.1:p.Tyr108Cys
NM_001114981.1:c.323A>G NP_001108453.1:p.Tyr108Cys
NM_001114982.1:c.323A>G NP_001108454.1:p.Tyr108Cys
NM_003722.4:c.605A>G NP_003713.3:p.Tyr202Cys
XM_005247843.2:c.605A>G XP_005247900.1:p.Tyr202Cys
XM_005247844.3:c.554A>G XP_005247901.1:p.Tyr185Cys
XM_005247846.2:c.605A>G XP_005247903.1:p.Tyr202Cys
XM_011513251.1:c.602A>G XP_011511553.1:p.Tyr201Cys
XM_011513252.1:c.599A>G XP_011511554.1:p.Tyr200Cys
XM_011513253.1:c.566A>G XP_011511555.1:p.Tyr189Cys
NM_001329144.1:c.605A>G NP_001316073.1:p.Tyr202Cys
NM_001329145.1:c.323A>G NP_001316074.1:p.Tyr108Cys
NM_001329146.1:c.68A>G NP_001316075.1:p.Tyr23Cys
NM_001329148.1:c.605A>G NP_001316077.1:p.Tyr202Cys
NM_001329149.1:c.323A>G NP_001316078.1:p.Tyr108Cys
NM_001329150.1:c.68A>G NP_001316079.1:p.Tyr23Cys
NM_001329964.1:c.599A>G NP_001316893.1:p.Tyr200Cys
NM_003722.5:c.605A>G MANE Select NP_003713.3:p.Tyr202Cys
NM_001114978.2:c.605A>G NP_001108450.1:p.Tyr202Cys
NM_001114979.2:c.605A>G NP_001108451.1:p.Tyr202Cys
NM_001114980.2:c.323A>G MANE Plus Clinical NP_001108452.1:p.Tyr108Cys
NM_001114981.2:c.323A>G NP_001108453.1:p.Tyr108Cys
NM_001114982.2:c.323A>G NP_001108454.1:p.Tyr108Cys
NM_001329144.2:c.605A>G NP_001316073.1:p.Tyr202Cys
NM_001329145.2:c.323A>G NP_001316074.1:p.Tyr108Cys
NM_001329146.2:c.68A>G NP_001316075.1:p.Tyr23Cys
NM_001329148.2:c.605A>G NP_001316077.1:p.Tyr202Cys
NM_001329149.2:c.323A>G NP_001316078.1:p.Tyr108Cys
NM_001329150.2:c.68A>G NP_001316079.1:p.Tyr23Cys
NM_001329964.2:c.599A>G NP_001316893.1:p.Tyr200Cys
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