Canonical Allele Identifier: CA1057617734

Gene: TP63

Linked Data

• dbSNP Id: rs1711531438
• gnomAD v3: 3-189638480-G-C
• gnomAD v4: 3-189638480-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189638480G>C , CM000665.2:g.189638480G>C	GRCh38
NC_000003.11:g.189356269G>C , CM000665.1:g.189356269G>C	GRCh37
NC_000003.10:g.190838963G>C	NCBI36
NG_007550.1:g.12054G>C
NG_007550.2:g.12054G>C
NG_007550.3:g.46735G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264731.8:c.62+6903G>C MANE Select	ENSP00000264731.3:n.62+6903G>C
ENST00000264731.7:c.62+6903G>C	ENSP00000264731.3:n.62+6903G>C
ENST00000320472.9:c.62+6903G>C	ENSP00000317510.5:n.62+6903G>C
ENST00000392460.7:c.62+6903G>C	ENSP00000376253.3:n.62+6903G>C
ENST00000418709.6:c.62+6903G>C	ENSP00000407144.2:n.62+6903G>C
ENST00000440651.6:c.62+6903G>C	ENSP00000394337.2:n.62+6903G>C
ENST00000486398.1:n.162+6903G>C
NM_001114978.1:c.62+6903G>C	NP_001108450.1:n.62+6903G>C
NM_001114979.1:c.62+6903G>C	NP_001108451.1:n.62+6903G>C
NM_003722.4:c.62+6903G>C	NP_003713.3:n.62+6903G>C
XM_005247843.2:c.62+6903G>C	XP_005247900.1:n.62+6903G>C
XM_005247844.3:c.11+7205G>C	XP_005247901.1:n.11+7205G>C
XM_005247846.2:c.62+6903G>C	XP_005247903.1:n.62+6903G>C
XM_011513251.1:c.59+15163G>C	XP_011511553.1:n.59+15163G>C
XM_011513252.1:c.56+41242G>C	XP_011511554.1:n.56+41242G>C
XM_011513253.1:c.23+71585G>C	XP_011511555.1:n.23+71585G>C
NM_001329144.1:c.62+6903G>C	NP_001316073.1:n.62+6903G>C
NM_001329148.1:c.62+6903G>C	NP_001316077.1:n.62+6903G>C
NM_001329964.1:c.56+41242G>C	NP_001316893.1:n.56+41242G>C
NM_003722.5:c.62+6903G>C MANE Select	NP_003713.3:n.62+6903G>C
NM_001114978.2:c.62+6903G>C	NP_001108450.1:n.62+6903G>C
NM_001114979.2:c.62+6903G>C	NP_001108451.1:n.62+6903G>C
NM_001329144.2:c.62+6903G>C	NP_001316073.1:n.62+6903G>C
NM_001329148.2:c.62+6903G>C	NP_001316077.1:n.62+6903G>C
NM_001329964.2:c.56+41242G>C	NP_001316893.1:n.56+41242G>C