Canonical Allele Identifier: CA904244490

Gene: TP63

Linked Data

• dbSNP Id: rs201395656
• gnomAD v3: 3-189897039-ATT-A
• gnomAD v4: 3-189897039-ATT-A
• MyVariant Identifiers: chr3:g.189614829_189614830del (hg19) ; chr3:g.189897040_189897041del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189897045_189897046del , CM000665.2:g.189897045_189897046del	GRCh38
NC_000003.11:g.189614834_189614835del , CM000665.1:g.189614834_189614835del	GRCh37
NC_000003.10:g.191097528_191097529del	NCBI36
NG_007550.1:g.270619_270620del
NG_007550.2:g.270619_270620del
NG_007550.3:g.305300_305301del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264731.8:c.*2543_*2544del MANE Select	ENSP00000264731.3:n.*2543_*2544del
ENST00000354600.10:c.*2543_*2544del MANE Plus Clinical	ENSP00000346614.5:n.*2543_*2544del
ENST00000264731.7:c.*2543_*2544del	ENSP00000264731.3:n.*2543_*2544del
ENST00000354600.9:c.*2543_*2544del	ENSP00000346614.5:n.*2543_*2544del
NM_001114978.1:c.*2824_*2825del	NP_001108450.1:n.*2824_*2825del
NM_001114980.1:c.*2543_*2544del	NP_001108452.1:n.*2543_*2544del
NM_001114981.1:c.*2824_*2825del	NP_001108453.1:n.*2824_*2825del
NM_003722.4:c.*2543_*2544del	NP_003713.3:n.*2543_*2544del
XM_005247843.2:c.*2543_*2544del	XP_005247900.1:n.*2543_*2544del
XM_005247844.3:c.*2543_*2544del	XP_005247901.1:n.*2543_*2544del
XM_011513251.1:c.*2543_*2544del	XP_011511553.1:n.*2543_*2544del
XM_011513252.1:c.*2543_*2544del	XP_011511554.1:n.*2543_*2544del
XM_011513253.1:c.*2543_*2544del	XP_011511555.1:n.*2543_*2544del
NM_001329144.1:c.*2814_*2815del	NP_001316073.1:n.*2814_*2815del
NM_001329145.1:c.*2814_*2815del	NP_001316074.1:n.*2814_*2815del
NM_001329146.1:c.*2543_*2544del	NP_001316075.1:n.*2543_*2544del
NM_001329148.1:c.*2543_*2544del	NP_001316077.1:n.*2543_*2544del
NM_001329149.1:c.*2814_*2815del	NP_001316078.1:n.*2814_*2815del
NM_001329150.1:c.*2814_*2815del	NP_001316079.1:n.*2814_*2815del
NM_001329964.1:c.*2543_*2544del	NP_001316893.1:n.*2543_*2544del
NM_003722.5:c.*2543_*2544del MANE Select	NP_003713.3:n.*2543_*2544del
NM_001114978.2:c.*2824_*2825del	NP_001108450.1:n.*2824_*2825del
NM_001114980.2:c.*2543_*2544del MANE Plus Clinical	NP_001108452.1:n.*2543_*2544del
NM_001114981.2:c.*2824_*2825del	NP_001108453.1:n.*2824_*2825del
NM_001329144.2:c.*2814_*2815del	NP_001316073.1:n.*2814_*2815del
NM_001329145.2:c.*2814_*2815del	NP_001316074.1:n.*2814_*2815del
NM_001329146.2:c.*2543_*2544del	NP_001316075.1:n.*2543_*2544del
NM_001329148.2:c.*2543_*2544del	NP_001316077.1:n.*2543_*2544del
NM_001329149.2:c.*2814_*2815del	NP_001316078.1:n.*2814_*2815del
NM_001329150.2:c.*2814_*2815del	NP_001316079.1:n.*2814_*2815del
NM_001329964.2:c.*2543_*2544del	NP_001316893.1:n.*2543_*2544del