Canonical Allele Identifier: CA1428536411

Gene: TP63

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189896976_189896977delinsCT , CM000665.2:g.189896976_189896977delinsCT	GRCh38
NC_000003.11:g.189614765_189614766delinsCT , CM000665.1:g.189614765_189614766delinsCT	GRCh37
NC_000003.10:g.191097459_191097460delinsCT	NCBI36
NG_007550.1:g.270550_270551delinsCT
NG_007550.2:g.270550_270551delinsCT
NG_007550.3:g.305231_305232delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264731.8:c.*2474_*2475delinsCT MANE Select	ENSP00000264731.3:n.*2474_*2475delinsCT
ENST00000354600.10:c.*2474_*2475delinsCT MANE Plus Clinical	ENSP00000346614.5:n.*2474_*2475delinsCT
ENST00000264731.7:c.*2474_*2475delinsCT	ENSP00000264731.3:n.*2474_*2475delinsCT
ENST00000354600.9:c.*2474_*2475delinsCT	ENSP00000346614.5:n.*2474_*2475delinsCT
NM_001114978.1:c.*2755_*2756delinsCT	NP_001108450.1:n.*2755_*2756delinsCT
NM_001114980.1:c.*2474_*2475delinsCT	NP_001108452.1:n.*2474_*2475delinsCT
NM_001114981.1:c.*2755_*2756delinsCT	NP_001108453.1:n.*2755_*2756delinsCT
NM_003722.4:c.*2474_*2475delinsCT	NP_003713.3:n.*2474_*2475delinsCT
XM_005247843.2:c.*2474_*2475delinsCT	XP_005247900.1:n.*2474_*2475delinsCT
XM_005247844.3:c.*2474_*2475delinsCT	XP_005247901.1:n.*2474_*2475delinsCT
XM_011513251.1:c.*2474_*2475delinsCT	XP_011511553.1:n.*2474_*2475delinsCT
XM_011513252.1:c.*2474_*2475delinsCT	XP_011511554.1:n.*2474_*2475delinsCT
XM_011513253.1:c.*2474_*2475delinsCT	XP_011511555.1:n.*2474_*2475delinsCT
NM_001329144.1:c.*2745_*2746delinsCT	NP_001316073.1:n.*2745_*2746delinsCT
NM_001329145.1:c.*2745_*2746delinsCT	NP_001316074.1:n.*2745_*2746delinsCT
NM_001329146.1:c.*2474_*2475delinsCT	NP_001316075.1:n.*2474_*2475delinsCT
NM_001329148.1:c.*2474_*2475delinsCT	NP_001316077.1:n.*2474_*2475delinsCT
NM_001329149.1:c.*2745_*2746delinsCT	NP_001316078.1:n.*2745_*2746delinsCT
NM_001329150.1:c.*2745_*2746delinsCT	NP_001316079.1:n.*2745_*2746delinsCT
NM_001329964.1:c.*2474_*2475delinsCT	NP_001316893.1:n.*2474_*2475delinsCT
NM_003722.5:c.*2474_*2475delinsCT MANE Select	NP_003713.3:n.*2474_*2475delinsCT
NM_001114978.2:c.*2755_*2756delinsCT	NP_001108450.1:n.*2755_*2756delinsCT
NM_001114980.2:c.*2474_*2475delinsCT MANE Plus Clinical	NP_001108452.1:n.*2474_*2475delinsCT
NM_001114981.2:c.*2755_*2756delinsCT	NP_001108453.1:n.*2755_*2756delinsCT
NM_001329144.2:c.*2745_*2746delinsCT	NP_001316073.1:n.*2745_*2746delinsCT
NM_001329145.2:c.*2745_*2746delinsCT	NP_001316074.1:n.*2745_*2746delinsCT
NM_001329146.2:c.*2474_*2475delinsCT	NP_001316075.1:n.*2474_*2475delinsCT
NM_001329148.2:c.*2474_*2475delinsCT	NP_001316077.1:n.*2474_*2475delinsCT
NM_001329149.2:c.*2745_*2746delinsCT	NP_001316078.1:n.*2745_*2746delinsCT
NM_001329150.2:c.*2745_*2746delinsCT	NP_001316079.1:n.*2745_*2746delinsCT
NM_001329964.2:c.*2474_*2475delinsCT	NP_001316893.1:n.*2474_*2475delinsCT