Canonical Allele Identifier: CA1428467820

Gene: TP63

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189789387_189789388delinsGT , CM000665.2:g.189789387_189789388delinsGT	GRCh38
NC_000003.11:g.189507176_189507177delinsGT , CM000665.1:g.189507176_189507177delinsGT	GRCh37
NC_000003.10:g.190989870_190989871delinsGT	NCBI36
NG_007550.1:g.162961_162962delinsGT
NG_007550.2:g.162961_162962delinsGT
NG_007550.3:g.197642_197643delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264731.8:c.325-18885_325-18884delinsGT MANE Select	ENSP00000264731.3:n.325-18885_325-18884delinsGT
ENST00000264731.7:c.325-18885_325-18884delinsGT	ENSP00000264731.3:n.325-18885_325-18884delinsGT
ENST00000320472.9:c.325-18885_325-18884delinsGT	ENSP00000317510.5:n.325-18885_325-18884delinsGT
ENST00000392460.7:c.325-18885_325-18884delinsGT	ENSP00000376253.3:n.325-18885_325-18884delinsGT
ENST00000418709.6:c.325-18885_325-18884delinsGT	ENSP00000407144.2:n.325-18885_325-18884delinsGT
ENST00000440651.6:c.325-18885_325-18884delinsGT	ENSP00000394337.2:n.325-18885_325-18884delinsGT
NM_001114978.1:c.325-18885_325-18884delinsGT	NP_001108450.1:n.325-18885_325-18884delinsGT
NM_001114979.1:c.325-18885_325-18884delinsGT	NP_001108451.1:n.325-18885_325-18884delinsGT
NM_003722.4:c.325-18885_325-18884delinsGT	NP_003713.3:n.325-18885_325-18884delinsGT
XM_005247843.2:c.325-18885_325-18884delinsGT	XP_005247900.1:n.325-18885_325-18884delinsGT
XM_005247844.3:c.274-18885_274-18884delinsGT	XP_005247901.1:n.274-18885_274-18884delinsGT
XM_005247846.2:c.325-18885_325-18884delinsGT	XP_005247903.1:n.325-18885_325-18884delinsGT
XM_011513251.1:c.322-18885_322-18884delinsGT	XP_011511553.1:n.322-18885_322-18884delinsGT
XM_011513252.1:c.319-18885_319-18884delinsGT	XP_011511554.1:n.319-18885_319-18884delinsGT
XM_011513253.1:c.286-18885_286-18884delinsGT	XP_011511555.1:n.286-18885_286-18884delinsGT
NM_001329144.1:c.325-18885_325-18884delinsGT	NP_001316073.1:n.325-18885_325-18884delinsGT
NM_001329148.1:c.325-18885_325-18884delinsGT	NP_001316077.1:n.325-18885_325-18884delinsGT
NM_001329964.1:c.319-18885_319-18884delinsGT	NP_001316893.1:n.319-18885_319-18884delinsGT
NM_003722.5:c.325-18885_325-18884delinsGT MANE Select	NP_003713.3:n.325-18885_325-18884delinsGT
NM_001114978.2:c.325-18885_325-18884delinsGT	NP_001108450.1:n.325-18885_325-18884delinsGT
NM_001114979.2:c.325-18885_325-18884delinsGT	NP_001108451.1:n.325-18885_325-18884delinsGT
NM_001329144.2:c.325-18885_325-18884delinsGT	NP_001316073.1:n.325-18885_325-18884delinsGT
NM_001329148.2:c.325-18885_325-18884delinsGT	NP_001316077.1:n.325-18885_325-18884delinsGT
NM_001329964.2:c.319-18885_319-18884delinsGT	NP_001316893.1:n.319-18885_319-18884delinsGT