Canonical Allele Identifier: CA340600

Gene: TP63

Linked Data

• ClinVar Variation Id: 6548
• ClinVar RCV Id: RCV000006923 ; RCV001280741
• dbSNP Id: rs113993966
• MyVariant Identifiers: chr3:g.189586385C>G (hg19) ; chr3:g.189868596C>G (hg38)
• PubMed: PMID:16724007 ; PMID:20556892

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189868596C>G , CM000665.2:g.189868596C>G	GRCh38
NC_000003.11:g.189586385C>G , CM000665.1:g.189586385C>G	GRCh37
NC_000003.10:g.191069079C>G	NCBI36
NG_007550.1:g.242170C>G
NG_007550.2:g.242170C>G
NG_007550.3:g.276851C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264731.8:c.1009C>G MANE Select	ENSP00000264731.3:p.Arg337Gly
ENST00000354600.10:c.727C>G MANE Plus Clinical	ENSP00000346614.5:p.Arg243Gly
ENST00000264731.7:c.1009C>G	ENSP00000264731.3:p.Arg337Gly
ENST00000320472.9:c.1009C>G	ENSP00000317510.5:p.Arg337Gly
ENST00000354600.9:c.727C>G	ENSP00000346614.5:p.Arg243Gly
ENST00000392460.7:c.1009C>G	ENSP00000376253.3:p.Arg337Gly
ENST00000392461.7:c.727C>G	ENSP00000376254.3:p.Arg243Gly
ENST00000392463.6:c.727C>G	ENSP00000376256.2:p.Arg243Gly
ENST00000418709.6:c.1009C>G	ENSP00000407144.2:p.Arg337Gly
ENST00000437221.5:c.727C>G	ENSP00000392488.1:p.Arg243Gly
ENST00000440651.6:c.1009C>G	ENSP00000394337.2:p.Arg337Gly
ENST00000449992.5:c.472C>G	ENSP00000387839.1:p.Arg158Gly
ENST00000456148.1:c.727C>G	ENSP00000389485.1:p.Arg243Gly
ENST00000460036.1:n.833C>G
NM_001114978.1:c.1009C>G	NP_001108450.1:p.Arg337Gly
NM_001114979.1:c.1009C>G	NP_001108451.1:p.Arg337Gly
NM_001114980.1:c.727C>G	NP_001108452.1:p.Arg243Gly
NM_001114981.1:c.727C>G	NP_001108453.1:p.Arg243Gly
NM_001114982.1:c.727C>G	NP_001108454.1:p.Arg243Gly
NM_003722.4:c.1009C>G	NP_003713.3:p.Arg337Gly
XM_005247843.2:c.1009C>G	XP_005247900.1:p.Arg337Gly
XM_005247844.3:c.958C>G	XP_005247901.1:p.Arg320Gly
XM_005247846.2:c.1009C>G	XP_005247903.1:p.Arg337Gly
XM_011513251.1:c.1006C>G	XP_011511553.1:p.Arg336Gly
XM_011513252.1:c.1003C>G	XP_011511554.1:p.Arg335Gly
XM_011513253.1:c.970C>G	XP_011511555.1:p.Arg324Gly
NM_001329144.1:c.1009C>G	NP_001316073.1:p.Arg337Gly
NM_001329145.1:c.727C>G	NP_001316074.1:p.Arg243Gly
NM_001329146.1:c.472C>G	NP_001316075.1:p.Arg158Gly
NM_001329148.1:c.1009C>G	NP_001316077.1:p.Arg337Gly
NM_001329149.1:c.727C>G	NP_001316078.1:p.Arg243Gly
NM_001329150.1:c.472C>G	NP_001316079.1:p.Arg158Gly
NM_001329964.1:c.1003C>G	NP_001316893.1:p.Arg335Gly
NM_003722.5:c.1009C>G MANE Select	NP_003713.3:p.Arg337Gly
NM_001114978.2:c.1009C>G	NP_001108450.1:p.Arg337Gly
NM_001114979.2:c.1009C>G	NP_001108451.1:p.Arg337Gly
NM_001114980.2:c.727C>G MANE Plus Clinical	NP_001108452.1:p.Arg243Gly
NM_001114981.2:c.727C>G	NP_001108453.1:p.Arg243Gly
NM_001114982.2:c.727C>G	NP_001108454.1:p.Arg243Gly
NM_001329144.2:c.1009C>G	NP_001316073.1:p.Arg337Gly
NM_001329145.2:c.727C>G	NP_001316074.1:p.Arg243Gly
NM_001329146.2:c.472C>G	NP_001316075.1:p.Arg158Gly
NM_001329148.2:c.1009C>G	NP_001316077.1:p.Arg337Gly
NM_001329149.2:c.727C>G	NP_001316078.1:p.Arg243Gly
NM_001329150.2:c.472C>G	NP_001316079.1:p.Arg158Gly
NM_001329964.2:c.1003C>G	NP_001316893.1:p.Arg335Gly