Canonical Allele Identifier: CA355759001

Gene: TP63

Linked Data

• MyVariant Identifiers: chr3:g.189608612G>T (hg19) ; chr3:g.189890823G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189890823G>T , CM000665.2:g.189890823G>T	GRCh38
NC_000003.11:g.189608612G>T , CM000665.1:g.189608612G>T	GRCh37
NC_000003.10:g.191091306G>T	NCBI36
NG_007550.1:g.264397G>T
NG_007550.2:g.264397G>T
NG_007550.3:g.299078G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264731.8:c.1687G>T MANE Select	ENSP00000264731.3:p.Asp563Tyr
ENST00000354600.10:c.1405G>T MANE Plus Clinical	ENSP00000346614.5:p.Asp469Tyr
ENST00000264731.7:c.1687G>T	ENSP00000264731.3:p.Asp563Tyr
ENST00000320472.9:c.1508-3383G>T	ENSP00000317510.5:n.1508-3383G>T
ENST00000354600.9:c.1405G>T	ENSP00000346614.5:p.Asp469Tyr
ENST00000392460.7:c.1652+1339G>T	ENSP00000376253.3:n.1652+1339G>T
ENST00000392461.7:c.1226-3383G>T	ENSP00000376254.3:n.1226-3383G>T
ENST00000392463.6:c.1370+1339G>T	ENSP00000376256.2:n.1370+1339G>T
ENST00000440651.6:c.1675G>T	ENSP00000394337.2:p.Asp559Tyr
ENST00000449992.5:c.1150G>T	ENSP00000387839.1:p.Asp384Tyr
ENST00000456148.1:c.1393G>T	ENSP00000389485.1:p.Asp465Tyr
NM_001114978.1:c.1652+1339G>T	NP_001108450.1:n.1652+1339G>T
NM_001114980.1:c.1405G>T	NP_001108452.1:p.Asp469Tyr
NM_001114981.1:c.1370+1339G>T	NP_001108453.1:n.1370+1339G>T
NM_003722.4:c.1687G>T	NP_003713.3:p.Asp563Tyr
XM_005247843.2:c.1675G>T	XP_005247900.1:p.Asp559Tyr
XM_005247844.3:c.1636G>T	XP_005247901.1:p.Asp546Tyr
XM_011513251.1:c.1684G>T	XP_011511553.1:p.Asp562Tyr
XM_011513252.1:c.1681G>T	XP_011511554.1:p.Asp561Tyr
XM_011513253.1:c.1648G>T	XP_011511555.1:p.Asp550Tyr
NM_001329144.1:c.1508-3383G>T	NP_001316073.1:n.1508-3383G>T
NM_001329145.1:c.1226-3383G>T	NP_001316074.1:n.1226-3383G>T
NM_001329146.1:c.1150G>T	NP_001316075.1:p.Asp384Tyr
NM_001329148.1:c.1675G>T	NP_001316077.1:p.Asp559Tyr
NM_001329149.1:c.1214-3383G>T	NP_001316078.1:n.1214-3383G>T
NM_001329150.1:c.959-3383G>T	NP_001316079.1:n.959-3383G>T
NM_001329964.1:c.1681G>T	NP_001316893.1:p.Asp561Tyr
NM_003722.5:c.1687G>T MANE Select	NP_003713.3:p.Asp563Tyr
NM_001114978.2:c.1652+1339G>T	NP_001108450.1:n.1652+1339G>T
NM_001114980.2:c.1405G>T MANE Plus Clinical	NP_001108452.1:p.Asp469Tyr
NM_001114981.2:c.1370+1339G>T	NP_001108453.1:n.1370+1339G>T
NM_001329144.2:c.1508-3383G>T	NP_001316073.1:n.1508-3383G>T
NM_001329145.2:c.1226-3383G>T	NP_001316074.1:n.1226-3383G>T
NM_001329146.2:c.1150G>T	NP_001316075.1:p.Asp384Tyr
NM_001329148.2:c.1675G>T	NP_001316077.1:p.Asp559Tyr
NM_001329149.2:c.1214-3383G>T	NP_001316078.1:n.1214-3383G>T
NM_001329150.2:c.959-3383G>T	NP_001316079.1:n.959-3383G>T
NM_001329964.2:c.1681G>T	NP_001316893.1:p.Asp561Tyr