Canonical Allele Identifier: CA2669041896

Gene: TP63

Linked Data

• gnomAD v4: 3-189864106-CCAGTAGTAAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189864110_189864119del , CM000665.2:g.189864110_189864119del	GRCh38
NC_000003.11:g.189581899_189581908del , CM000665.1:g.189581899_189581908del	GRCh37
NC_000003.10:g.191064593_191064602del	NCBI36
NG_007550.1:g.237684_237693del
NG_007550.2:g.237684_237693del
NG_007550.3:g.272365_272374del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264731.8:c.580-122_580-113del MANE Select	ENSP00000264731.3:n.580-122_580-113del
ENST00000354600.10:c.298-122_298-113del MANE Plus Clinical	ENSP00000346614.5:n.298-122_298-113del
ENST00000264731.7:c.580-122_580-113del	ENSP00000264731.3:n.580-122_580-113del
ENST00000320472.9:c.580-122_580-113del	ENSP00000317510.5:n.580-122_580-113del
ENST00000354600.9:c.298-122_298-113del	ENSP00000346614.5:n.298-122_298-113del
ENST00000392460.7:c.580-122_580-113del	ENSP00000376253.3:n.580-122_580-113del
ENST00000392461.7:c.298-122_298-113del	ENSP00000376254.3:n.298-122_298-113del
ENST00000392463.6:c.298-122_298-113del	ENSP00000376256.2:n.298-122_298-113del
ENST00000418709.6:c.580-122_580-113del	ENSP00000407144.2:n.580-122_580-113del
ENST00000434928.5:c.514-122_514-113del	ENSP00000401661.1:n.514-122_514-113del
ENST00000437221.5:c.298-122_298-113del	ENSP00000392488.1:n.298-122_298-113del
ENST00000440651.6:c.580-122_580-113del	ENSP00000394337.2:n.580-122_580-113del
ENST00000449992.5:c.43-122_43-113del	ENSP00000387839.1:n.43-122_43-113del
ENST00000456148.1:c.298-122_298-113del	ENSP00000389485.1:n.298-122_298-113del
ENST00000460036.1:n.404-122_404-113del
NM_001114978.1:c.580-122_580-113del	NP_001108450.1:n.580-122_580-113del
NM_001114979.1:c.580-122_580-113del	NP_001108451.1:n.580-122_580-113del
NM_001114980.1:c.298-122_298-113del	NP_001108452.1:n.298-122_298-113del
NM_001114981.1:c.298-122_298-113del	NP_001108453.1:n.298-122_298-113del
NM_001114982.1:c.298-122_298-113del	NP_001108454.1:n.298-122_298-113del
NM_003722.4:c.580-122_580-113del	NP_003713.3:n.580-122_580-113del
XM_005247843.2:c.580-122_580-113del	XP_005247900.1:n.580-122_580-113del
XM_005247844.3:c.529-122_529-113del	XP_005247901.1:n.529-122_529-113del
XM_005247846.2:c.580-122_580-113del	XP_005247903.1:n.580-122_580-113del
XM_011513251.1:c.577-122_577-113del	XP_011511553.1:n.577-122_577-113del
XM_011513252.1:c.574-122_574-113del	XP_011511554.1:n.574-122_574-113del
XM_011513253.1:c.541-122_541-113del	XP_011511555.1:n.541-122_541-113del
NM_001329144.1:c.580-122_580-113del	NP_001316073.1:n.580-122_580-113del
NM_001329145.1:c.298-122_298-113del	NP_001316074.1:n.298-122_298-113del
NM_001329146.1:c.43-122_43-113del	NP_001316075.1:n.43-122_43-113del
NM_001329148.1:c.580-122_580-113del	NP_001316077.1:n.580-122_580-113del
NM_001329149.1:c.298-122_298-113del	NP_001316078.1:n.298-122_298-113del
NM_001329150.1:c.43-122_43-113del	NP_001316079.1:n.43-122_43-113del
NM_001329964.1:c.574-122_574-113del	NP_001316893.1:n.574-122_574-113del
NM_003722.5:c.580-122_580-113del MANE Select	NP_003713.3:n.580-122_580-113del
NM_001114978.2:c.580-122_580-113del	NP_001108450.1:n.580-122_580-113del
NM_001114979.2:c.580-122_580-113del	NP_001108451.1:n.580-122_580-113del
NM_001114980.2:c.298-122_298-113del MANE Plus Clinical	NP_001108452.1:n.298-122_298-113del
NM_001114981.2:c.298-122_298-113del	NP_001108453.1:n.298-122_298-113del
NM_001114982.2:c.298-122_298-113del	NP_001108454.1:n.298-122_298-113del
NM_001329144.2:c.580-122_580-113del	NP_001316073.1:n.580-122_580-113del
NM_001329145.2:c.298-122_298-113del	NP_001316074.1:n.298-122_298-113del
NM_001329146.2:c.43-122_43-113del	NP_001316075.1:n.43-122_43-113del
NM_001329148.2:c.580-122_580-113del	NP_001316077.1:n.580-122_580-113del
NM_001329149.2:c.298-122_298-113del	NP_001316078.1:n.298-122_298-113del
NM_001329150.2:c.43-122_43-113del	NP_001316079.1:n.43-122_43-113del
NM_001329964.2:c.574-122_574-113del	NP_001316893.1:n.574-122_574-113del