Canonical Allele Identifier: CA355751101

Gene: TP63

Linked Data

• dbSNP Id: rs1560310855
• MyVariant Identifiers: chr3:g.189611997T>A (hg19) ; chr3:g.189894208T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189894208T>A , CM000665.2:g.189894208T>A	GRCh38
NC_000003.11:g.189611997T>A , CM000665.1:g.189611997T>A	GRCh37
NC_000003.10:g.191094691T>A	NCBI36
NG_007550.1:g.267782T>A
NG_007550.2:g.267782T>A
NG_007550.3:g.302463T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264731.8:c.1749T>A MANE Select	ENSP00000264731.3:p.Asp583Glu
ENST00000354600.10:c.1467T>A MANE Plus Clinical	ENSP00000346614.5:p.Asp489Glu
ENST00000264731.7:c.1749T>A	ENSP00000264731.3:p.Asp583Glu
ENST00000320472.9:c.1510T>A	ENSP00000317510.5:p.Ser504Thr
ENST00000354600.9:c.1467T>A	ENSP00000346614.5:p.Asp489Glu
ENST00000392460.7:c.1655T>A	ENSP00000376253.3:p.Ile552Asn
ENST00000392461.7:c.1228T>A	ENSP00000376254.3:p.Ser410Thr
ENST00000392463.6:c.1373T>A	ENSP00000376256.2:p.Ile458Asn
ENST00000440651.6:c.1737T>A	ENSP00000394337.2:p.Asp579Glu
ENST00000449992.5:c.1212T>A	ENSP00000387839.1:p.Asp404Glu
ENST00000456148.1:c.1455T>A	ENSP00000389485.1:p.Asp485Glu
NM_001114978.1:c.1655T>A	NP_001108450.1:p.Ile552Asn
NM_001114980.1:c.1467T>A	NP_001108452.1:p.Asp489Glu
NM_001114981.1:c.1373T>A	NP_001108453.1:p.Ile458Asn
NM_003722.4:c.1749T>A	NP_003713.3:p.Asp583Glu
XM_005247843.2:c.1737T>A	XP_005247900.1:p.Asp579Glu
XM_005247844.3:c.1698T>A	XP_005247901.1:p.Asp566Glu
XM_011513251.1:c.1746T>A	XP_011511553.1:p.Asp582Glu
XM_011513252.1:c.1743T>A	XP_011511554.1:p.Asp581Glu
XM_011513253.1:c.1710T>A	XP_011511555.1:p.Asp570Glu
NM_001329144.1:c.1510T>A	NP_001316073.1:p.Ser504Thr
NM_001329145.1:c.1228T>A	NP_001316074.1:p.Ser410Thr
NM_001329146.1:c.1212T>A	NP_001316075.1:p.Asp404Glu
NM_001329148.1:c.1737T>A	NP_001316077.1:p.Asp579Glu
NM_001329149.1:c.1216T>A	NP_001316078.1:p.Ser406Thr
NM_001329150.1:c.961T>A	NP_001316079.1:p.Ser321Thr
NM_001329964.1:c.1743T>A	NP_001316893.1:p.Asp581Glu
NM_003722.5:c.1749T>A MANE Select	NP_003713.3:p.Asp583Glu
NM_001114978.2:c.1655T>A	NP_001108450.1:p.Ile552Asn
NM_001114980.2:c.1467T>A MANE Plus Clinical	NP_001108452.1:p.Asp489Glu
NM_001114981.2:c.1373T>A	NP_001108453.1:p.Ile458Asn
NM_001329144.2:c.1510T>A	NP_001316073.1:p.Ser504Thr
NM_001329145.2:c.1228T>A	NP_001316074.1:p.Ser410Thr
NM_001329146.2:c.1212T>A	NP_001316075.1:p.Asp404Glu
NM_001329148.2:c.1737T>A	NP_001316077.1:p.Asp579Glu
NM_001329149.2:c.1216T>A	NP_001316078.1:p.Ser406Thr
NM_001329150.2:c.961T>A	NP_001316079.1:p.Ser321Thr
NM_001329964.2:c.1743T>A	NP_001316893.1:p.Asp581Glu