Canonical Allele Identifier: CA16604493
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 379663
ClinVar RCV Id: RCV000437272
dbSNP Id: rs1057520683
MyVariant Identifiers: chr3:g.189507590A>G (hg19) chr3:g.189789801A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.189789801A>G , CM000665.2:g.189789801A>G GRCh38
NC_000003.11:g.189507590A>G , CM000665.1:g.189507590A>G GRCh37
NC_000003.10:g.190990284A>G NCBI36
NG_007550.1:g.163375A>G
NG_007550.2:g.163375A>G
NG_007550.3:g.198056A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264731.8:c.325-18471A>G MANE Select ENSP00000264731.3:n.325-18471A>G
ENST00000354600.10:c.1A>G MANE Plus Clinical ENSP00000346614.5:p.Met1Val
ENST00000264731.7:c.325-18471A>G ENSP00000264731.3:n.325-18471A>G
ENST00000320472.9:c.325-18471A>G ENSP00000317510.5:n.325-18471A>G
ENST00000354600.9:c.1A>G ENSP00000346614.5:p.Met1Val
ENST00000392460.7:c.325-18471A>G ENSP00000376253.3:n.325-18471A>G
ENST00000392461.7:c.1A>G ENSP00000376254.3:p.Met1Val
ENST00000392463.6:c.1A>G ENSP00000376256.2:p.Met1Val
ENST00000418709.6:c.325-18471A>G ENSP00000407144.2:n.325-18471A>G
ENST00000434928.5:c.1A>G ENSP00000401661.1:p.Met1Val
ENST00000437221.5:c.1A>G ENSP00000392488.1:p.Met1Val
ENST00000440651.6:c.325-18471A>G ENSP00000394337.2:n.325-18471A>G
ENST00000449992.5:c.1A>G ENSP00000387839.1:p.Met1Val
ENST00000456148.1:c.1A>G ENSP00000389485.1:p.Met1Val
ENST00000460036.1:n.107A>G
NM_001114978.1:c.325-18471A>G NP_001108450.1:n.325-18471A>G
NM_001114979.1:c.325-18471A>G NP_001108451.1:n.325-18471A>G
NM_001114980.1:c.1A>G NP_001108452.1:p.Met1Val
NM_001114981.1:c.1A>G NP_001108453.1:p.Met1Val
NM_001114982.1:c.1A>G NP_001108454.1:p.Met1Val
NM_003722.4:c.325-18471A>G NP_003713.3:n.325-18471A>G
XM_005247843.2:c.325-18471A>G XP_005247900.1:n.325-18471A>G
XM_005247844.3:c.274-18471A>G XP_005247901.1:n.274-18471A>G
XM_005247846.2:c.325-18471A>G XP_005247903.1:n.325-18471A>G
XM_011513251.1:c.322-18471A>G XP_011511553.1:n.322-18471A>G
XM_011513252.1:c.319-18471A>G XP_011511554.1:n.319-18471A>G
XM_011513253.1:c.286-18471A>G XP_011511555.1:n.286-18471A>G
NM_001329144.1:c.325-18471A>G NP_001316073.1:n.325-18471A>G
NM_001329145.1:c.1A>G NP_001316074.1:p.Met1Val
NM_001329146.1:c.1A>G NP_001316075.1:p.Met1Val
NM_001329148.1:c.325-18471A>G NP_001316077.1:n.325-18471A>G
NM_001329149.1:c.1A>G NP_001316078.1:p.Met1Val
NM_001329150.1:c.1A>G NP_001316079.1:p.Met1Val
NM_001329964.1:c.319-18471A>G NP_001316893.1:n.319-18471A>G
NM_003722.5:c.325-18471A>G MANE Select NP_003713.3:n.325-18471A>G
NM_001114978.2:c.325-18471A>G NP_001108450.1:n.325-18471A>G
NM_001114979.2:c.325-18471A>G NP_001108451.1:n.325-18471A>G
NM_001114980.2:c.1A>G MANE Plus Clinical NP_001108452.1:p.Met1Val
NM_001114981.2:c.1A>G NP_001108453.1:p.Met1Val
NM_001114982.2:c.1A>G NP_001108454.1:p.Met1Val
NM_001329144.2:c.325-18471A>G NP_001316073.1:n.325-18471A>G
NM_001329145.2:c.1A>G NP_001316074.1:p.Met1Val
NM_001329146.2:c.1A>G NP_001316075.1:p.Met1Val
NM_001329148.2:c.325-18471A>G NP_001316077.1:n.325-18471A>G
NM_001329149.2:c.1A>G NP_001316078.1:p.Met1Val
NM_001329150.2:c.1A>G NP_001316079.1:p.Met1Val
NM_001329964.2:c.319-18471A>G NP_001316893.1:n.319-18471A>G
Search 100 bp 5'
Search 100 bp 3'