Canonical Allele Identifier: CA658657360

Gene: TP63

Linked Data

• ClinVar Variation Id: 449513
• ClinVar RCV Id: RCV000522243
• dbSNP Id: rs1553840705
• MyVariant Identifiers: chr3:g.189507615del (hg19) ; chr3:g.189789826del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189789826del , CM000665.2:g.189789826del	GRCh38
NC_000003.11:g.189507615del , CM000665.1:g.189507615del	GRCh37
NC_000003.10:g.190990309del	NCBI36
NG_007550.1:g.163400del
NG_007550.2:g.163400del
NG_007550.3:g.198081del

Transcript Alleles

HGVS	Amino-acid change
ENST00000264731.8:c.325-18446del MANE Select	ENSP00000264731.3:n.325-18446del
ENST00000354600.10:c.26del MANE Plus Clinical	ENSP00000346614.5:p.Gln9ArgfsTer15
ENST00000264731.7:c.325-18446del	ENSP00000264731.3:n.325-18446del
ENST00000320472.9:c.325-18446del	ENSP00000317510.5:n.325-18446del
ENST00000354600.9:c.26del	ENSP00000346614.5:p.Gln9ArgfsTer15
ENST00000392460.7:c.325-18446del	ENSP00000376253.3:n.325-18446del
ENST00000392461.7:c.26del	ENSP00000376254.3:p.Gln9ArgfsTer15
ENST00000392463.6:c.26del	ENSP00000376256.2:p.Gln9ArgfsTer15
ENST00000418709.6:c.325-18446del	ENSP00000407144.2:n.325-18446del
ENST00000434928.5:c.26del	ENSP00000401661.1:p.Gln9ArgfsTer15
ENST00000437221.5:c.26del	ENSP00000392488.1:p.Gln9ArgfsTer15
ENST00000440651.6:c.325-18446del	ENSP00000394337.2:n.325-18446del
ENST00000449992.5:c.26del	ENSP00000387839.1:p.Gln9ArgfsTer11
ENST00000456148.1:c.26del	ENSP00000389485.1:p.Gln9ArgfsTer15
ENST00000460036.1:n.132del
NM_001114978.1:c.325-18446del	NP_001108450.1:n.325-18446del
NM_001114979.1:c.325-18446del	NP_001108451.1:n.325-18446del
NM_001114980.1:c.26del	NP_001108452.1:p.Gln9ArgfsTer15
NM_001114981.1:c.26del	NP_001108453.1:p.Gln9ArgfsTer15
NM_001114982.1:c.26del	NP_001108454.1:p.Gln9ArgfsTer15
NM_003722.4:c.325-18446del	NP_003713.3:n.325-18446del
XM_005247843.2:c.325-18446del	XP_005247900.1:n.325-18446del
XM_005247844.3:c.274-18446del	XP_005247901.1:n.274-18446del
XM_005247846.2:c.325-18446del	XP_005247903.1:n.325-18446del
XM_011513251.1:c.322-18446del	XP_011511553.1:n.322-18446del
XM_011513252.1:c.319-18446del	XP_011511554.1:n.319-18446del
XM_011513253.1:c.286-18446del	XP_011511555.1:n.286-18446del
NM_001329144.1:c.325-18446del	NP_001316073.1:n.325-18446del
NM_001329145.1:c.26del	NP_001316074.1:p.Gln9ArgfsTer15
NM_001329146.1:c.26del	NP_001316075.1:p.Gln9ArgfsTer11
NM_001329148.1:c.325-18446del	NP_001316077.1:n.325-18446del
NM_001329149.1:c.26del	NP_001316078.1:p.Gln9ArgfsTer15
NM_001329150.1:c.26del	NP_001316079.1:p.Gln9ArgfsTer11
NM_001329964.1:c.319-18446del	NP_001316893.1:n.319-18446del
NM_003722.5:c.325-18446del MANE Select	NP_003713.3:n.325-18446del
NM_001114978.2:c.325-18446del	NP_001108450.1:n.325-18446del
NM_001114979.2:c.325-18446del	NP_001108451.1:n.325-18446del
NM_001114980.2:c.26del MANE Plus Clinical	NP_001108452.1:p.Gln9ArgfsTer15
NM_001114981.2:c.26del	NP_001108453.1:p.Gln9ArgfsTer15
NM_001114982.2:c.26del	NP_001108454.1:p.Gln9ArgfsTer15
NM_001329144.2:c.325-18446del	NP_001316073.1:n.325-18446del
NM_001329145.2:c.26del	NP_001316074.1:p.Gln9ArgfsTer15
NM_001329146.2:c.26del	NP_001316075.1:p.Gln9ArgfsTer11
NM_001329148.2:c.325-18446del	NP_001316077.1:n.325-18446del
NM_001329149.2:c.26del	NP_001316078.1:p.Gln9ArgfsTer15
NM_001329150.2:c.26del	NP_001316079.1:p.Gln9ArgfsTer11
NM_001329964.2:c.319-18446del	NP_001316893.1:n.319-18446del