Canonical Allele Identifier: CA915949519
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 660287
ClinVar RCV Id: RCV000817451
dbSNP Id: rs1597360140

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7673687_7673704del , CM000679.2:g.7673687_7673704del GRCh38
NC_000017.10:g.7577005_7577022del , CM000679.1:g.7577005_7577022del GRCh37
NC_000017.9:g.7517730_7517747del NCBI36
NG_017013.2:g.18848_18865del , LRG_321:g.18848_18865del

Transcript Alleles

HGVS Amino-acid change
ENST00000503591.2:c.917_919+15del
ENST00000508793.6:c.917_919+15del
ENST00000509690.6:c.521_523+15del
ENST00000514944.6:c.638_640+15del
ENST00000604348.6:c.896_898+15del
ENST00000269305.9:c.917_919+15del
ENST00000269305.8:c.917_919+15del
ENST00000359597.8:c.917_919+15del
ENST00000413465.6:c.782+478_782+495del ENSP00000410739.2:n.782+478_782+495del
ENST00000420246.6:c.917_919+15del
ENST00000445888.6:c.917_919+15del
ENST00000455263.6:c.917_919+15del
ENST00000504290.5:c.521_523+15del
ENST00000504937.5:c.521_523+15del
ENST00000509690.5:c.521_523+15del
ENST00000510385.5:c.521_523+15del
ENST00000610292.4:c.800_802+15del
ENST00000610538.4:c.800_802+15del
ENST00000610623.4:c.440_442+15del
ENST00000615910.4:c.884_886+15del
ENST00000617185.4:c.917_919+15del
ENST00000618944.4:c.440_442+15del
ENST00000619186.4:c.440_442+15del
ENST00000619485.4:c.800_802+15del
ENST00000620739.4:c.800_802+15del
ENST00000622645.4:c.800_802+15del
ENST00000635293.1:c.800_802+15del
NM_000546.5:c.917_919+15del , LRG_321t1:c.917_919+15del
NM_001126112.2:c.917_919+15del , LRG_321t2:c.917_919+15del
NM_001126113.2:c.917_919+15del , LRG_321t4:c.917_919+15del
NM_001126114.2:c.917_919+15del , LRG_321t3:c.917_919+15del
NM_001126115.1:c.521_523+15del , LRG_321t5:c.521_523+15del
NM_001126116.1:c.521_523+15del , LRG_321t6:c.521_523+15del
NM_001126117.1:c.521_523+15del , LRG_321t7:c.521_523+15del
NM_001126118.1:c.800_802+15del , LRG_321t8:c.800_802+15del
NM_001276695.1:c.800_802+15del
NM_001276696.1:c.800_802+15del
NM_001276697.1:c.440_442+15del
NM_001276698.1:c.440_442+15del
NM_001276699.1:c.440_442+15del
NM_001276760.1:c.800_802+15del
NM_001276761.1:c.800_802+15del
NM_001276695.2:c.800_802+15del
NM_001276696.2:c.800_802+15del
NM_001276697.2:c.440_442+15del
NM_001276698.2:c.440_442+15del
NM_001276699.2:c.440_442+15del
NM_001276760.2:c.800_802+15del
NM_001276761.2:c.800_802+15del
NM_000546.6:c.917_919+15del
NM_001126112.3:c.917_919+15del
NM_001126113.3:c.917_919+15del
NM_001126114.3:c.917_919+15del
NM_001126115.2:c.521_523+15del
NM_001126116.2:c.521_523+15del
NM_001126117.2:c.521_523+15del
NM_001126118.2:c.800_802+15del
NM_001276695.3:c.800_802+15del
NM_001276696.3:c.800_802+15del
NM_001276697.3:c.440_442+15del
NM_001276698.3:c.440_442+15del
NM_001276699.3:c.440_442+15del
NM_001276760.3:c.800_802+15del
NM_001276761.3:c.800_802+15del