Canonical Allele Identifier: CA397831830

Gene: TP53

Linked Data

• ClinVar Variation Id: 568955
• ClinVar RCV Id: RCV000689466 ; RCV002289965 ; RCV001176639
• dbSNP Id: rs1567541711
• gnomAD v4: 17-7670618-G-A
• MyVariant Identifiers: chr17:g.7573936G>A (hg19) ; chr17:g.7670618G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7670618G>A , CM000679.2:g.7670618G>A	GRCh38
NC_000017.10:g.7573936G>A , CM000679.1:g.7573936G>A	GRCh37
NC_000017.9:g.7514661G>A	NCBI36
NG_017013.2:g.21933C>T , LRG_321:g.21933C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503591.2:c.1091C>T	ENSP00000426252.2:p.Ala364Val
ENST00000508793.6:c.1091C>T	ENSP00000424104.2:p.Ala364Val
ENST00000509690.6:c.695C>T	ENSP00000425104.2:p.Ala232Val
ENST00000514944.6:c.812C>T	ENSP00000423862.2:p.Ala271Val
ENST00000604348.6:c.1070C>T	ENSP00000473895.2:p.Ala357Val
ENST00000269305.9:c.1091C>T MANE Select	ENSP00000269305.4:p.Ala364Val
ENST00000269305.8:c.1091C>T	ENSP00000269305.4:p.Ala364Val
ENST00000359597.8:c.993+2917C>T	ENSP00000352610.4:n.993+2917C>T
ENST00000413465.6:c.782+3563C>T	ENSP00000410739.2:n.782+3563C>T
ENST00000420246.6:c.*198C>T	ENSP00000391127.2:n.*198C>T
ENST00000445888.6:c.1091C>T	ENSP00000391478.2:p.Ala364Val
ENST00000455263.6:c.*110C>T	ENSP00000398846.2:n.*110C>T
ENST00000504290.5:c.*110C>T	ENSP00000484409.1:n.*110C>T
ENST00000504937.5:c.695C>T	ENSP00000481179.1:p.Ala232Val
ENST00000510385.5:c.*198C>T	ENSP00000478499.1:n.*198C>T
ENST00000576024.1:c.54-928C>T
ENST00000610292.4:c.974C>T	ENSP00000478219.1:p.Ala325Val
ENST00000610538.4:c.*110C>T	ENSP00000480868.1:n.*110C>T
ENST00000610623.4:c.*110C>T	ENSP00000477531.1:n.*110C>T
ENST00000615910.4:c.1058C>T	ENSP00000482903.1:p.Ala353Val
ENST00000617185.4:c.*198C>T	ENSP00000482258.1:n.*198C>T
ENST00000618944.4:c.*198C>T	ENSP00000481401.1:n.*198C>T
ENST00000619186.4:c.614C>T	ENSP00000484375.1:p.Ala205Val
ENST00000619485.4:c.974C>T	ENSP00000482537.1:p.Ala325Val
ENST00000620739.4:c.974C>T	ENSP00000481638.1:p.Ala325Val
ENST00000622645.4:c.*198C>T	ENSP00000482222.1:n.*198C>T
ENST00000635293.1:c.974C>T	ENSP00000488924.1:p.Ala325Val
NM_000546.5:c.1091C>T , LRG_321t1:c.1091C>T	NP_000537.3:p.Ala364Val
NM_001126112.2:c.1091C>T , LRG_321t2:c.1091C>T	NP_001119584.1:p.Ala364Val
NM_001126113.2:c.*110C>T , LRG_321t4:c.*110C>T	NP_001119585.1:n.*110C>T
NM_001126114.2:c.*198C>T , LRG_321t3:c.*198C>T	NP_001119586.1:n.*198C>T
NM_001126115.1:c.695C>T , LRG_321t5:c.695C>T	NP_001119587.1:p.Ala232Val
NM_001126116.1:c.*198C>T , LRG_321t6:c.*198C>T	NP_001119588.1:n.*198C>T
NM_001126117.1:c.*110C>T , LRG_321t7:c.*110C>T	NP_001119589.1:n.*110C>T
NM_001126118.1:c.974C>T , LRG_321t8:c.974C>T	NP_001119590.1:p.Ala325Val
NM_001276695.1:c.*110C>T	NP_001263624.1:n.*110C>T
NM_001276696.1:c.*198C>T	NP_001263625.1:n.*198C>T
NM_001276697.1:c.614C>T	NP_001263626.1:p.Ala205Val
NM_001276698.1:c.*198C>T	NP_001263627.1:n.*198C>T
NM_001276699.1:c.*110C>T	NP_001263628.1:n.*110C>T
NM_001276760.1:c.974C>T	NP_001263689.1:p.Ala325Val
NM_001276761.1:c.974C>T	NP_001263690.1:p.Ala325Val
NM_001276695.2:c.*110C>T	NP_001263624.1:n.*110C>T
NM_001276696.2:c.*198C>T	NP_001263625.1:n.*198C>T
NM_001276697.2:c.614C>T	NP_001263626.1:p.Ala205Val
NM_001276698.2:c.*198C>T	NP_001263627.1:n.*198C>T
NM_001276699.2:c.*110C>T	NP_001263628.1:n.*110C>T
NM_001276760.2:c.974C>T	NP_001263689.1:p.Ala325Val
NM_001276761.2:c.974C>T	NP_001263690.1:p.Ala325Val
NM_000546.6:c.1091C>T MANE Select	NP_000537.3:p.Ala364Val
NM_001126112.3:c.1091C>T	NP_001119584.1:p.Ala364Val
NM_001126113.3:c.*110C>T	NP_001119585.1:n.*110C>T
NM_001126114.3:c.*198C>T	NP_001119586.1:n.*198C>T
NM_001126115.2:c.695C>T	NP_001119587.1:p.Ala232Val
NM_001126116.2:c.*198C>T	NP_001119588.1:n.*198C>T
NM_001126117.2:c.*110C>T	NP_001119589.1:n.*110C>T
NM_001126118.2:c.974C>T	NP_001119590.1:p.Ala325Val
NM_001276695.3:c.*110C>T	NP_001263624.1:n.*110C>T
NM_001276696.3:c.*198C>T	NP_001263625.1:n.*198C>T
NM_001276697.3:c.614C>T	NP_001263626.1:p.Ala205Val
NM_001276698.3:c.*198C>T	NP_001263627.1:n.*198C>T
NM_001276699.3:c.*110C>T	NP_001263628.1:n.*110C>T
NM_001276760.3:c.974C>T	NP_001263689.1:p.Ala325Val
NM_001276761.3:c.974C>T	NP_001263690.1:p.Ala325Val