Canonical Allele Identifier: CA2573136832

Gene: TP63

Linked Data

• ClinVar Variation Id: 1684042
• ClinVar RCV Id: RCV002244562
• dbSNP Id: rs2108638585

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189808510_189808518del , CM000665.2:g.189808510_189808518del	GRCh38
NC_000003.11:g.189526299_189526307del , CM000665.1:g.189526299_189526307del	GRCh37
NC_000003.10:g.191008993_191009001del	NCBI36
NG_007550.1:g.182084_182092del
NG_007550.2:g.182084_182092del
NG_007550.3:g.216765_216773del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264731.8:c.563_571del MANE Select	ENSP00000264731.3:p.Lys188_Ala190del
ENST00000354600.10:c.281_289del MANE Plus Clinical	ENSP00000346614.5:p.Lys94_Ala96del
ENST00000264731.7:c.563_571del	ENSP00000264731.3:p.Lys188_Ala190del
ENST00000320472.9:c.563_571del	ENSP00000317510.5:p.Lys188_Ala190del
ENST00000354600.9:c.281_289del	ENSP00000346614.5:p.Lys94_Ala96del
ENST00000392460.7:c.563_571del	ENSP00000376253.3:p.Lys188_Ala190del
ENST00000392461.7:c.281_289del	ENSP00000376254.3:p.Lys94_Ala96del
ENST00000392463.6:c.281_289del	ENSP00000376256.2:p.Lys94_Ala96del
ENST00000418709.6:c.563_571del	ENSP00000407144.2:p.Lys188_Ala190del
ENST00000434928.5:c.281_289del	ENSP00000401661.1:p.Lys94_Ala96del
ENST00000437221.5:c.281_289del	ENSP00000392488.1:p.Lys94_Ala96del
ENST00000440651.6:c.563_571del	ENSP00000394337.2:p.Lys188_Ala190del
ENST00000449992.5:c.42+18668_42+18676del	ENSP00000387839.1:n.42+18668_42+18676del
ENST00000456148.1:c.281_289del	ENSP00000389485.1:p.Lys94_Ala96del
ENST00000460036.1:n.387_395del
NM_001114978.1:c.563_571del	NP_001108450.1:p.Lys188_Ala190del
NM_001114979.1:c.563_571del	NP_001108451.1:p.Lys188_Ala190del
NM_001114980.1:c.281_289del	NP_001108452.1:p.Lys94_Ala96del
NM_001114981.1:c.281_289del	NP_001108453.1:p.Lys94_Ala96del
NM_001114982.1:c.281_289del	NP_001108454.1:p.Lys94_Ala96del
NM_003722.4:c.563_571del	NP_003713.3:p.Lys188_Ala190del
XM_005247843.2:c.563_571del	XP_005247900.1:p.Lys188_Ala190del
XM_005247844.3:c.512_520del	XP_005247901.1:p.Lys171_Ala173del
XM_005247846.2:c.563_571del	XP_005247903.1:p.Lys188_Ala190del
XM_011513251.1:c.560_568del	XP_011511553.1:p.Lys187_Ala189del
XM_011513252.1:c.557_565del	XP_011511554.1:p.Lys186_Ala188del
XM_011513253.1:c.524_532del	XP_011511555.1:p.Lys175_Ala177del
NM_001329144.1:c.563_571del	NP_001316073.1:p.Lys188_Ala190del
NM_001329145.1:c.281_289del	NP_001316074.1:p.Lys94_Ala96del
NM_001329146.1:c.42+18668_42+18676del	NP_001316075.1:n.42+18668_42+18676del
NM_001329148.1:c.563_571del	NP_001316077.1:p.Lys188_Ala190del
NM_001329149.1:c.281_289del	NP_001316078.1:p.Lys94_Ala96del
NM_001329150.1:c.42+18668_42+18676del	NP_001316079.1:n.42+18668_42+18676del
NM_001329964.1:c.557_565del	NP_001316893.1:p.Lys186_Ala188del
NM_003722.5:c.563_571del MANE Select	NP_003713.3:p.Lys188_Ala190del
NM_001114978.2:c.563_571del	NP_001108450.1:p.Lys188_Ala190del
NM_001114979.2:c.563_571del	NP_001108451.1:p.Lys188_Ala190del
NM_001114980.2:c.281_289del MANE Plus Clinical	NP_001108452.1:p.Lys94_Ala96del
NM_001114981.2:c.281_289del	NP_001108453.1:p.Lys94_Ala96del
NM_001114982.2:c.281_289del	NP_001108454.1:p.Lys94_Ala96del
NM_001329144.2:c.563_571del	NP_001316073.1:p.Lys188_Ala190del
NM_001329145.2:c.281_289del	NP_001316074.1:p.Lys94_Ala96del
NM_001329146.2:c.42+18668_42+18676del	NP_001316075.1:n.42+18668_42+18676del
NM_001329148.2:c.563_571del	NP_001316077.1:p.Lys188_Ala190del
NM_001329149.2:c.281_289del	NP_001316078.1:p.Lys94_Ala96del
NM_001329150.2:c.42+18668_42+18676del	NP_001316079.1:n.42+18668_42+18676del
NM_001329964.2:c.557_565del	NP_001316893.1:p.Lys186_Ala188del