Canonical Allele Identifier: CA913187862

Gene: TP53

Linked Data

• ClinVar Variation Id: 628384
• ClinVar RCV Id: RCV000772844
• dbSNP Id: rs1567557864
• gnomAD v4: 17-7676464-A-AGGGGGCTGGGGTTGGGGT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7676470_7676487dup , CM000679.2:g.7676470_7676487dup	GRCh38
NC_000017.10:g.7579788_7579805dup , CM000679.1:g.7579788_7579805dup	GRCh37
NC_000017.9:g.7520513_7520530dup	NCBI36
NG_017013.2:g.16069_16086dup , LRG_321:g.16069_16086dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000503591.2:c.74+39_74+56dup	ENSP00000426252.2:n.74+39_74+56dup
ENST00000508793.6:c.74+39_74+56dup	ENSP00000424104.2:n.74+39_74+56dup
ENST00000509690.6:c.-21-1246_-21-1229dup	ENSP00000425104.2:n.-21-1246_-21-1229dup
ENST00000514944.6:c.74+39_74+56dup	ENSP00000423862.2:n.74+39_74+56dup
ENST00000604348.6:c.74+39_74+56dup	ENSP00000473895.2:n.74+39_74+56dup
ENST00000269305.9:c.74+39_74+56dup MANE Select	ENSP00000269305.4:n.74+39_74+56dup
ENST00000269305.8:c.74+39_74+56dup	ENSP00000269305.4:n.74+39_74+56dup
ENST00000359597.8:c.74+39_74+56dup	ENSP00000352610.4:n.74+39_74+56dup
ENST00000413465.6:c.74+39_74+56dup	ENSP00000410739.2:n.74+39_74+56dup
ENST00000420246.6:c.74+39_74+56dup	ENSP00000391127.2:n.74+39_74+56dup
ENST00000445888.6:c.74+39_74+56dup	ENSP00000391478.2:n.74+39_74+56dup
ENST00000455263.6:c.74+39_74+56dup	ENSP00000398846.2:n.74+39_74+56dup
ENST00000503591.1:c.74+39_74+56dup	ENSP00000426252.1:n.74+39_74+56dup
ENST00000505014.5:n.252_269dup
ENST00000508793.5:c.74+39_74+56dup	ENSP00000424104.1:n.74+39_74+56dup
ENST00000509690.5:c.-21-1246_-21-1229dup	ENSP00000425104.1:n.-21-1246_-21-1229dup
ENST00000514944.5:c.74+39_74+56dup	ENSP00000423862.1:n.74+39_74+56dup
ENST00000604348.5:c.74+39_74+56dup	ENSP00000473895.1:n.74+39_74+56dup
ENST00000610292.4:c.-122_-105dup	ENSP00000478219.1:n.-122_-105dup
ENST00000610538.4:c.-44+39_-44+56dup	ENSP00000480868.1:n.-44+39_-44+56dup
ENST00000615910.4:c.74+39_74+56dup	ENSP00000482903.1:n.74+39_74+56dup
ENST00000617185.4:c.74+39_74+56dup	ENSP00000482258.1:n.74+39_74+56dup
ENST00000619485.4:c.-44+39_-44+56dup	ENSP00000482537.1:n.-44+39_-44+56dup
ENST00000620739.4:c.-44+39_-44+56dup	ENSP00000481638.1:n.-44+39_-44+56dup
ENST00000622645.4:c.-44+39_-44+56dup	ENSP00000482222.1:n.-44+39_-44+56dup
ENST00000635293.1:c.-44+39_-44+56dup	ENSP00000488924.1:n.-44+39_-44+56dup
NM_000546.5:c.74+39_74+56dup , LRG_321t1:c.74+39_74+56dup	NP_000537.3:n.74+39_74+56dup
NM_001126112.2:c.74+39_74+56dup , LRG_321t2:c.74+39_74+56dup	NP_001119584.1:n.74+39_74+56dup
NM_001126113.2:c.74+39_74+56dup , LRG_321t4:c.74+39_74+56dup	NP_001119585.1:n.74+39_74+56dup
NM_001126114.2:c.74+39_74+56dup , LRG_321t3:c.74+39_74+56dup	NP_001119586.1:n.74+39_74+56dup
NM_001126118.1:c.-122_-105dup , LRG_321t8:c.-122_-105dup	NP_001119590.1:n.-122_-105dup
NM_001276695.1:c.-44+39_-44+56dup	NP_001263624.1:n.-44+39_-44+56dup
NM_001276696.1:c.-44+39_-44+56dup	NP_001263625.1:n.-44+39_-44+56dup
NM_001276760.1:c.-44+39_-44+56dup	NP_001263689.1:n.-44+39_-44+56dup
NM_001276761.1:c.-44+39_-44+56dup	NP_001263690.1:n.-44+39_-44+56dup
NM_001276695.2:c.-44+39_-44+56dup	NP_001263624.1:n.-44+39_-44+56dup
NM_001276696.2:c.-44+39_-44+56dup	NP_001263625.1:n.-44+39_-44+56dup
NM_001276760.2:c.-44+39_-44+56dup	NP_001263689.1:n.-44+39_-44+56dup
NM_001276761.2:c.-44+39_-44+56dup	NP_001263690.1:n.-44+39_-44+56dup
NM_000546.6:c.74+39_74+56dup MANE Select	NP_000537.3:n.74+39_74+56dup
NM_001126112.3:c.74+39_74+56dup	NP_001119584.1:n.74+39_74+56dup
NM_001126113.3:c.74+39_74+56dup	NP_001119585.1:n.74+39_74+56dup
NM_001126114.3:c.74+39_74+56dup	NP_001119586.1:n.74+39_74+56dup
NM_001126118.2:c.-122_-105dup	NP_001119590.1:n.-122_-105dup
NM_001276695.3:c.-44+39_-44+56dup	NP_001263624.1:n.-44+39_-44+56dup
NM_001276696.3:c.-44+39_-44+56dup	NP_001263625.1:n.-44+39_-44+56dup
NM_001276760.3:c.-44+39_-44+56dup	NP_001263689.1:n.-44+39_-44+56dup
NM_001276761.3:c.-44+39_-44+56dup	NP_001263690.1:n.-44+39_-44+56dup