Canonical Allele Identifier: CA437416433

Gene: TP63

Linked Data

• MyVariant Identifiers: chr3:g.189608587G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189890798G>T , CM000665.2:g.189890798G>T	GRCh38
NC_000003.11:g.189608587G>T , CM000665.1:g.189608587G>T	GRCh37
NC_000003.10:g.191091281G>T	NCBI36
NG_007550.1:g.264372G>T
NG_007550.2:g.264372G>T
NG_007550.3:g.299053G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264731.8:c.1662G>T MANE Select	ENSP00000264731.3:p.Ala554=
ENST00000354600.10:c.1380G>T MANE Plus Clinical	ENSP00000346614.5:p.Ala460=
ENST00000264731.7:c.1662G>T	ENSP00000264731.3:p.Ala554=
ENST00000320472.9:c.1508-3408G>T	ENSP00000317510.5:n.1508-3408G>T
ENST00000354600.9:c.1380G>T	ENSP00000346614.5:p.Ala460=
ENST00000392460.7:c.1652+1314G>T	ENSP00000376253.3:n.1652+1314G>T
ENST00000392461.7:c.1226-3408G>T	ENSP00000376254.3:n.1226-3408G>T
ENST00000392463.6:c.1370+1314G>T	ENSP00000376256.2:n.1370+1314G>T
ENST00000440651.6:c.1650G>T	ENSP00000394337.2:p.Ala550=
ENST00000449992.5:c.1125G>T	ENSP00000387839.1:p.Ala375=
ENST00000456148.1:c.1368G>T	ENSP00000389485.1:p.Ala456=
NM_001114978.1:c.1652+1314G>T	NP_001108450.1:n.1652+1314G>T
NM_001114980.1:c.1380G>T	NP_001108452.1:p.Ala460=
NM_001114981.1:c.1370+1314G>T	NP_001108453.1:n.1370+1314G>T
NM_003722.4:c.1662G>T	NP_003713.3:p.Ala554=
XM_005247843.2:c.1650G>T	XP_005247900.1:p.Ala550=
XM_005247844.3:c.1611G>T	XP_005247901.1:p.Ala537=
XM_011513251.1:c.1659G>T	XP_011511553.1:p.Ala553=
XM_011513252.1:c.1656G>T	XP_011511554.1:p.Ala552=
XM_011513253.1:c.1623G>T	XP_011511555.1:p.Ala541=
NM_001329144.1:c.1508-3408G>T	NP_001316073.1:n.1508-3408G>T
NM_001329145.1:c.1226-3408G>T	NP_001316074.1:n.1226-3408G>T
NM_001329146.1:c.1125G>T	NP_001316075.1:p.Ala375=
NM_001329148.1:c.1650G>T	NP_001316077.1:p.Ala550=
NM_001329149.1:c.1214-3408G>T	NP_001316078.1:n.1214-3408G>T
NM_001329150.1:c.959-3408G>T	NP_001316079.1:n.959-3408G>T
NM_001329964.1:c.1656G>T	NP_001316893.1:p.Ala552=
NM_003722.5:c.1662G>T MANE Select	NP_003713.3:p.Ala554=
NM_001114978.2:c.1652+1314G>T	NP_001108450.1:n.1652+1314G>T
NM_001114980.2:c.1380G>T MANE Plus Clinical	NP_001108452.1:p.Ala460=
NM_001114981.2:c.1370+1314G>T	NP_001108453.1:n.1370+1314G>T
NM_001329144.2:c.1508-3408G>T	NP_001316073.1:n.1508-3408G>T
NM_001329145.2:c.1226-3408G>T	NP_001316074.1:n.1226-3408G>T
NM_001329146.2:c.1125G>T	NP_001316075.1:p.Ala375=
NM_001329148.2:c.1650G>T	NP_001316077.1:p.Ala550=
NM_001329149.2:c.1214-3408G>T	NP_001316078.1:n.1214-3408G>T
NM_001329150.2:c.959-3408G>T	NP_001316079.1:n.959-3408G>T
NM_001329964.2:c.1656G>T	NP_001316893.1:p.Ala552=