Canonical Allele Identifier: CA3099384791
Community Standard Title: NM_003722.5(TP63):c.1846C= (p.Leu616=)
Gene: TP63 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.189894305C= , CM000665.2:g.189894305C= GRCh38
NC_000003.11:g.189612094C= , CM000665.1:g.189612094C= GRCh37
NC_000003.10:g.191094788C= NCBI36
NG_007550.1:g.267879C=
NG_007550.2:g.267879C=
NG_007550.3:g.302560C=

Transcript Alleles

HGVS Amino-acid Change
NM_003722.5:c.1846C= MANE Select NP_003713.3:p.Leu616=
ENST00000264731.8:c.1846C= MANE Select ENSP00000264731.3:p.Leu616=
NM_001114980.2:c.1564C= MANE Plus Clinical NP_001108452.1:p.Leu522=
ENST00000354600.10:c.1564C= MANE Plus Clinical ENSP00000346614.5:p.Leu522=
NM_001114978.1:c.*84C= NP_001108450.1:n.*84C=
NM_001114978.2:c.*84C= NP_001108450.1:n.*84C=
NM_001114980.1:c.1564C= NP_001108452.1:p.Leu522=
NM_001114981.1:c.*84C= NP_001108453.1:n.*84C=
NM_001114981.2:c.*84C= NP_001108453.1:n.*84C=
NM_001329144.1:c.*74C= NP_001316073.1:n.*74C=
NM_001329144.2:c.*74C= NP_001316073.1:n.*74C=
NM_001329145.1:c.*74C= NP_001316074.1:n.*74C=
NM_001329145.2:c.*74C= NP_001316074.1:n.*74C=
NM_001329146.1:c.1309C= NP_001316075.1:p.Leu437=
NM_001329146.2:c.1309C= NP_001316075.1:p.Leu437=
NM_001329148.1:c.1834C= NP_001316077.1:p.Leu612=
NM_001329148.2:c.1834C= NP_001316077.1:p.Leu612=
NM_001329149.1:c.*74C= NP_001316078.1:n.*74C=
NM_001329149.2:c.*74C= NP_001316078.1:n.*74C=
NM_001329150.1:c.*74C= NP_001316079.1:n.*74C=
NM_001329150.2:c.*74C= NP_001316079.1:n.*74C=
NM_001329964.1:c.1840C= NP_001316893.1:p.Leu614=
NM_001329964.2:c.1840C= NP_001316893.1:p.Leu614=
NM_003722.4:c.1846C= NP_003713.3:p.Leu616=
ENST00000264731.7:c.1846C= ENSP00000264731.3:p.Leu616=
ENST00000320472.9:c.*74C= ENSP00000317510.5:n.*74C=
ENST00000354600.9:c.1564C= ENSP00000346614.5:p.Leu522=
ENST00000440651.6:c.1834C= ENSP00000394337.2:p.Leu612=
ENST00000449992.5:c.1309C= ENSP00000387839.1:p.Leu437=
ENST00000456148.1:c.1552C= ENSP00000389485.1:p.Leu518=
XM_005247843.2:c.1834C= XP_005247900.1:p.Leu612=
XM_005247844.3:c.1795C= XP_005247901.1:p.Leu599=
XM_011513251.1:c.1843C= XP_011511553.1:p.Leu615=
XM_011513252.1:c.1840C= XP_011511554.1:p.Leu614=
XM_011513253.1:c.1807C= XP_011511555.1:p.Leu603=