Canonical Allele Identifier: CA2752590

Gene: TP63

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189894336T>G , CM000665.2:g.189894336T>G	GRCh38
NC_000003.11:g.189612125T>G , CM000665.1:g.189612125T>G	GRCh37
NC_000003.10:g.191094819T>G	NCBI36
NG_007550.1:g.267910T>G
NG_007550.2:g.267910T>G
NG_007550.3:g.302591T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_003722.5:c.1877T>G MANE Select	NP_003713.3:p.Val626Gly
ENST00000264731.8:c.1877T>G MANE Select	ENSP00000264731.3:p.Val626Gly
NM_001114980.2:c.1595T>G MANE Plus Clinical	NP_001108452.1:p.Val532Gly
ENST00000354600.10:c.1595T>G MANE Plus Clinical	ENSP00000346614.5:p.Val532Gly
NM_001114978.1:c.*115T>G	NP_001108450.1:n.*115T>G
NM_001114978.2:c.*115T>G	NP_001108450.1:n.*115T>G
NM_001114980.1:c.1595T>G	NP_001108452.1:p.Val532Gly
NM_001114981.1:c.*115T>G	NP_001108453.1:n.*115T>G
NM_001114981.2:c.*115T>G	NP_001108453.1:n.*115T>G
NM_001329144.1:c.*105T>G	NP_001316073.1:n.*105T>G
NM_001329144.2:c.*105T>G	NP_001316073.1:n.*105T>G
NM_001329145.1:c.*105T>G	NP_001316074.1:n.*105T>G
NM_001329145.2:c.*105T>G	NP_001316074.1:n.*105T>G
NM_001329146.1:c.1340T>G	NP_001316075.1:p.Val447Gly
NM_001329146.2:c.1340T>G	NP_001316075.1:p.Val447Gly
NM_001329148.1:c.1865T>G	NP_001316077.1:p.Val622Gly
NM_001329148.2:c.1865T>G	NP_001316077.1:p.Val622Gly
NM_001329149.1:c.*105T>G	NP_001316078.1:n.*105T>G
NM_001329149.2:c.*105T>G	NP_001316078.1:n.*105T>G
NM_001329150.1:c.*105T>G	NP_001316079.1:n.*105T>G
NM_001329150.2:c.*105T>G	NP_001316079.1:n.*105T>G
NM_001329964.1:c.1871T>G	NP_001316893.1:p.Val624Gly
NM_001329964.2:c.1871T>G	NP_001316893.1:p.Val624Gly
NM_003722.4:c.1877T>G	NP_003713.3:p.Val626Gly
ENST00000264731.7:c.1877T>G	ENSP00000264731.3:p.Val626Gly
ENST00000320472.9:c.*105T>G	ENSP00000317510.5:n.*105T>G
ENST00000354600.9:c.1595T>G	ENSP00000346614.5:p.Val532Gly
ENST00000440651.6:c.1865T>G	ENSP00000394337.2:p.Val622Gly
ENST00000449992.5:c.1340T>G	ENSP00000387839.1:p.Val447Gly
ENST00000456148.1:c.1583T>G	ENSP00000389485.1:p.Val528Gly
XM_005247843.2:c.1865T>G	XP_005247900.1:p.Val622Gly
XM_005247844.3:c.1826T>G	XP_005247901.1:p.Val609Gly
XM_011513251.1:c.1874T>G	XP_011511553.1:p.Val625Gly
XM_011513252.1:c.1871T>G	XP_011511554.1:p.Val624Gly
XM_011513253.1:c.1838T>G	XP_011511555.1:p.Val613Gly