Canonical Allele Identifier: CA2580094895

Gene: TP53

Linked Data

• ClinVar Variation Id: 2450756
• ClinVar RCV Id: RCV003177181

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7673533_7673541delinsTA , CM000679.2:g.7673533_7673541delinsTA	GRCh38
NC_000017.10:g.7576851_7576859delinsTA , CM000679.1:g.7576851_7576859delinsTA	GRCh37
NC_000017.9:g.7517576_7517584delinsTA	NCBI36
NG_017013.2:g.19010_19018delinsTA , LRG_321:g.19010_19018delinsTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000503591.2:c.987_993+2delinsTA
ENST00000508793.6:c.987_993+2delinsTA
ENST00000509690.6:c.591_597+2delinsTA
ENST00000514944.6:c.708_714+2delinsTA
ENST00000604348.6:c.966_972+2delinsTA
ENST00000269305.9:c.987_993+2delinsTA
ENST00000269305.8:c.987_993+2delinsTA
ENST00000359597.8:c.987_993+2delinsTA
ENST00000413465.6:c.782+640_782+648delinsTA	ENSP00000410739.2:n.782+640_782+648delins...
ENST00000420246.6:c.987_993+2delinsTA
ENST00000445888.6:c.987_993+2delinsTA
ENST00000455263.6:c.987_993+2delinsTA
ENST00000504290.5:c.591_597+2delinsTA
ENST00000504937.5:c.591_597+2delinsTA
ENST00000510385.5:c.591_597+2delinsTA
ENST00000576024.1:c.47_53+2delinsTA
ENST00000610292.4:c.870_876+2delinsTA
ENST00000610538.4:c.870_876+2delinsTA
ENST00000610623.4:c.510_516+2delinsTA
ENST00000615910.4:c.954_960+2delinsTA
ENST00000617185.4:c.987_993+2delinsTA
ENST00000618944.4:c.510_516+2delinsTA
ENST00000619186.4:c.510_516+2delinsTA
ENST00000619485.4:c.870_876+2delinsTA
ENST00000620739.4:c.870_876+2delinsTA
ENST00000622645.4:c.870_876+2delinsTA
ENST00000635293.1:c.870_876+2delinsTA
NM_000546.5:c.987_993+2delinsTA , LRG_321t1:c.987_993+2delinsTA
NM_001126112.2:c.987_993+2delinsTA , LRG_321t2:c.987_993+2delinsTA
NM_001126113.2:c.987_993+2delinsTA , LRG_321t4:c.987_993+2delinsTA
NM_001126114.2:c.987_993+2delinsTA , LRG_321t3:c.987_993+2delinsTA
NM_001126115.1:c.591_597+2delinsTA , LRG_321t5:c.591_597+2delinsTA
NM_001126116.1:c.591_597+2delinsTA , LRG_321t6:c.591_597+2delinsTA
NM_001126117.1:c.591_597+2delinsTA , LRG_321t7:c.591_597+2delinsTA
NM_001126118.1:c.870_876+2delinsTA , LRG_321t8:c.870_876+2delinsTA
NM_001276695.1:c.870_876+2delinsTA
NM_001276696.1:c.870_876+2delinsTA
NM_001276697.1:c.510_516+2delinsTA
NM_001276698.1:c.510_516+2delinsTA
NM_001276699.1:c.510_516+2delinsTA
NM_001276760.1:c.870_876+2delinsTA
NM_001276761.1:c.870_876+2delinsTA
NM_001276695.2:c.870_876+2delinsTA
NM_001276696.2:c.870_876+2delinsTA
NM_001276697.2:c.510_516+2delinsTA
NM_001276698.2:c.510_516+2delinsTA
NM_001276699.2:c.510_516+2delinsTA
NM_001276760.2:c.870_876+2delinsTA
NM_001276761.2:c.870_876+2delinsTA
NM_000546.6:c.987_993+2delinsTA
NM_001126112.3:c.987_993+2delinsTA
NM_001126113.3:c.987_993+2delinsTA
NM_001126114.3:c.987_993+2delinsTA
NM_001126115.2:c.591_597+2delinsTA
NM_001126116.2:c.591_597+2delinsTA
NM_001126117.2:c.591_597+2delinsTA
NM_001126118.2:c.870_876+2delinsTA
NM_001276695.3:c.870_876+2delinsTA
NM_001276696.3:c.870_876+2delinsTA
NM_001276697.3:c.510_516+2delinsTA
NM_001276698.3:c.510_516+2delinsTA
NM_001276699.3:c.510_516+2delinsTA
NM_001276760.3:c.870_876+2delinsTA
NM_001276761.3:c.870_876+2delinsTA