Canonical Allele Identifier: CA355751118

Gene: TP63

Linked Data

• dbSNP Id: rs2108872937
• gnomAD v4: 3-189894213-C-T
• MyVariant Identifiers: chr3:g.189612002C>T (hg19) ; chr3:g.189894213C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189894213C>T , CM000665.2:g.189894213C>T	GRCh38
NC_000003.11:g.189612002C>T , CM000665.1:g.189612002C>T	GRCh37
NC_000003.10:g.191094696C>T	NCBI36
NG_007550.1:g.267787C>T
NG_007550.2:g.267787C>T
NG_007550.3:g.302468C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264731.8:c.1754C>T MANE Select	ENSP00000264731.3:p.Ala585Val
ENST00000354600.10:c.1472C>T MANE Plus Clinical	ENSP00000346614.5:p.Ala491Val
ENST00000264731.7:c.1754C>T	ENSP00000264731.3:p.Ala585Val
ENST00000320472.9:c.1515C>T	ENSP00000317510.5:p.Gly505=
ENST00000354600.9:c.1472C>T	ENSP00000346614.5:p.Ala491Val
ENST00000392460.7:c.1660C>T	ENSP00000376253.3:p.Gln554Ter
ENST00000392461.7:c.1233C>T	ENSP00000376254.3:p.Gly411=
ENST00000392463.6:c.1378C>T	ENSP00000376256.2:p.Gln460Ter
ENST00000440651.6:c.1742C>T	ENSP00000394337.2:p.Ala581Val
ENST00000449992.5:c.1217C>T	ENSP00000387839.1:p.Ala406Val
ENST00000456148.1:c.1460C>T	ENSP00000389485.1:p.Ala487Val
NM_001114978.1:c.1660C>T	NP_001108450.1:p.Gln554Ter
NM_001114980.1:c.1472C>T	NP_001108452.1:p.Ala491Val
NM_001114981.1:c.1378C>T	NP_001108453.1:p.Gln460Ter
NM_003722.4:c.1754C>T	NP_003713.3:p.Ala585Val
XM_005247843.2:c.1742C>T	XP_005247900.1:p.Ala581Val
XM_005247844.3:c.1703C>T	XP_005247901.1:p.Ala568Val
XM_011513251.1:c.1751C>T	XP_011511553.1:p.Ala584Val
XM_011513252.1:c.1748C>T	XP_011511554.1:p.Ala583Val
XM_011513253.1:c.1715C>T	XP_011511555.1:p.Ala572Val
NM_001329144.1:c.1515C>T	NP_001316073.1:p.Gly505=
NM_001329145.1:c.1233C>T	NP_001316074.1:p.Gly411=
NM_001329146.1:c.1217C>T	NP_001316075.1:p.Ala406Val
NM_001329148.1:c.1742C>T	NP_001316077.1:p.Ala581Val
NM_001329149.1:c.1221C>T	NP_001316078.1:p.Gly407=
NM_001329150.1:c.966C>T	NP_001316079.1:p.Gly322=
NM_001329964.1:c.1748C>T	NP_001316893.1:p.Ala583Val
NM_003722.5:c.1754C>T MANE Select	NP_003713.3:p.Ala585Val
NM_001114978.2:c.1660C>T	NP_001108450.1:p.Gln554Ter
NM_001114980.2:c.1472C>T MANE Plus Clinical	NP_001108452.1:p.Ala491Val
NM_001114981.2:c.1378C>T	NP_001108453.1:p.Gln460Ter
NM_001329144.2:c.1515C>T	NP_001316073.1:p.Gly505=
NM_001329145.2:c.1233C>T	NP_001316074.1:p.Gly411=
NM_001329146.2:c.1217C>T	NP_001316075.1:p.Ala406Val
NM_001329148.2:c.1742C>T	NP_001316077.1:p.Ala581Val
NM_001329149.2:c.1221C>T	NP_001316078.1:p.Gly407=
NM_001329150.2:c.966C>T	NP_001316079.1:p.Gly322=
NM_001329964.2:c.1748C>T	NP_001316893.1:p.Ala583Val