Canonical Allele Identifier: CA904195362

Gene: TP63

Linked Data

• dbSNP Id: rs1255373193
• gnomAD v3: 3-189638403-G-A
• gnomAD v4: 3-189638403-G-A
• MyVariant Identifiers: chr3:g.189356192G>A (hg19) ; chr3:g.189638403G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189638403G>A , CM000665.2:g.189638403G>A	GRCh38
NC_000003.11:g.189356192G>A , CM000665.1:g.189356192G>A	GRCh37
NC_000003.10:g.190838886G>A	NCBI36
NG_007550.1:g.11977G>A
NG_007550.2:g.11977G>A
NG_007550.3:g.46658G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264731.8:c.62+6826G>A MANE Select	ENSP00000264731.3:n.62+6826G>A
ENST00000264731.7:c.62+6826G>A	ENSP00000264731.3:n.62+6826G>A
ENST00000320472.9:c.62+6826G>A	ENSP00000317510.5:n.62+6826G>A
ENST00000392460.7:c.62+6826G>A	ENSP00000376253.3:n.62+6826G>A
ENST00000418709.6:c.62+6826G>A	ENSP00000407144.2:n.62+6826G>A
ENST00000440651.6:c.62+6826G>A	ENSP00000394337.2:n.62+6826G>A
ENST00000486398.1:n.162+6826G>A
NM_001114978.1:c.62+6826G>A	NP_001108450.1:n.62+6826G>A
NM_001114979.1:c.62+6826G>A	NP_001108451.1:n.62+6826G>A
NM_003722.4:c.62+6826G>A	NP_003713.3:n.62+6826G>A
XM_005247843.2:c.62+6826G>A	XP_005247900.1:n.62+6826G>A
XM_005247844.3:c.11+7128G>A	XP_005247901.1:n.11+7128G>A
XM_005247846.2:c.62+6826G>A	XP_005247903.1:n.62+6826G>A
XM_011513251.1:c.59+15086G>A	XP_011511553.1:n.59+15086G>A
XM_011513252.1:c.56+41165G>A	XP_011511554.1:n.56+41165G>A
XM_011513253.1:c.23+71508G>A	XP_011511555.1:n.23+71508G>A
NM_001329144.1:c.62+6826G>A	NP_001316073.1:n.62+6826G>A
NM_001329148.1:c.62+6826G>A	NP_001316077.1:n.62+6826G>A
NM_001329964.1:c.56+41165G>A	NP_001316893.1:n.56+41165G>A
NM_003722.5:c.62+6826G>A MANE Select	NP_003713.3:n.62+6826G>A
NM_001114978.2:c.62+6826G>A	NP_001108450.1:n.62+6826G>A
NM_001114979.2:c.62+6826G>A	NP_001108451.1:n.62+6826G>A
NM_001329144.2:c.62+6826G>A	NP_001316073.1:n.62+6826G>A
NM_001329148.2:c.62+6826G>A	NP_001316077.1:n.62+6826G>A
NM_001329964.2:c.56+41165G>A	NP_001316893.1:n.56+41165G>A