Canonical Allele Identifier: CA16617859
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 418521
ClinVar RCV Id: RCV000485320
dbSNP Id: rs1064793283
MyVariant Identifiers: chr3:g.189612170C>T (hg19) chr3:g.189894381C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.189894381C>T , CM000665.2:g.189894381C>T GRCh38
NC_000003.11:g.189612170C>T , CM000665.1:g.189612170C>T GRCh37
NC_000003.10:g.191094864C>T NCBI36
NG_007550.1:g.267955C>T
NG_007550.2:g.267955C>T
NG_007550.3:g.302636C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264731.8:c.1922C>T MANE Select ENSP00000264731.3:p.Ala641Val
ENST00000354600.10:c.1640C>T MANE Plus Clinical ENSP00000346614.5:p.Ala547Val
ENST00000264731.7:c.1922C>T ENSP00000264731.3:p.Ala641Val
ENST00000320472.9:c.*150C>T ENSP00000317510.5:n.*150C>T
ENST00000354600.9:c.1640C>T ENSP00000346614.5:p.Ala547Val
ENST00000440651.6:c.1910C>T ENSP00000394337.2:p.Ala637Val
ENST00000449992.5:c.1385C>T ENSP00000387839.1:p.Ala462Val
ENST00000456148.1:c.1628C>T ENSP00000389485.1:p.Ala543Val
NM_001114978.1:c.*160C>T NP_001108450.1:n.*160C>T
NM_001114980.1:c.1640C>T NP_001108452.1:p.Ala547Val
NM_001114981.1:c.*160C>T NP_001108453.1:n.*160C>T
NM_003722.4:c.1922C>T NP_003713.3:p.Ala641Val
XM_005247843.2:c.1910C>T XP_005247900.1:p.Ala637Val
XM_005247844.3:c.1871C>T XP_005247901.1:p.Ala624Val
XM_011513251.1:c.1919C>T XP_011511553.1:p.Ala640Val
XM_011513252.1:c.1916C>T XP_011511554.1:p.Ala639Val
XM_011513253.1:c.1883C>T XP_011511555.1:p.Ala628Val
NM_001329144.1:c.*150C>T NP_001316073.1:n.*150C>T
NM_001329145.1:c.*150C>T NP_001316074.1:n.*150C>T
NM_001329146.1:c.1385C>T NP_001316075.1:p.Ala462Val
NM_001329148.1:c.1910C>T NP_001316077.1:p.Ala637Val
NM_001329149.1:c.*150C>T NP_001316078.1:n.*150C>T
NM_001329150.1:c.*150C>T NP_001316079.1:n.*150C>T
NM_001329964.1:c.1916C>T NP_001316893.1:p.Ala639Val
NM_003722.5:c.1922C>T MANE Select NP_003713.3:p.Ala641Val
NM_001114978.2:c.*160C>T NP_001108450.1:n.*160C>T
NM_001114980.2:c.1640C>T MANE Plus Clinical NP_001108452.1:p.Ala547Val
NM_001114981.2:c.*160C>T NP_001108453.1:n.*160C>T
NM_001329144.2:c.*150C>T NP_001316073.1:n.*150C>T
NM_001329145.2:c.*150C>T NP_001316074.1:n.*150C>T
NM_001329146.2:c.1385C>T NP_001316075.1:p.Ala462Val
NM_001329148.2:c.1910C>T NP_001316077.1:p.Ala637Val
NM_001329149.2:c.*150C>T NP_001316078.1:n.*150C>T
NM_001329150.2:c.*150C>T NP_001316079.1:n.*150C>T
NM_001329964.2:c.1916C>T NP_001316893.1:p.Ala639Val
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