Linked Data
ClinVar Variation Id:
325645
dbSNP Id:
rs886053515
gnomAD v3:
17-7687442-G-A
gnomAD v4:
17-7687442-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7687442G>A , CM000679.2:g.7687442G>A | GRCh38 |
| NC_000017.10:g.7590760G>A , CM000679.1:g.7590760G>A | GRCh37 |
| NC_000017.9:g.7531485G>A | NCBI36 |
| NG_017013.2:g.5109C>T , LRG_321:g.5109C>T | |
| NG_028245.1:g.6372G>A , LRG_375:g.6372G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000509690.6:c.-87C>T (TP53) | ENSP00000425104.2:n.-87C>T | |
| ENST00000571370.2:n.82C>T (TP53) | ||
| ENST00000604348.6:c.-94C>T (TP53) | ENSP00000473895.2:n.-94C>T | |
| ENST00000269305.9:c.-94C>T (TP53) MANE Select | ENSP00000269305.4:n.-94C>T | |
| ENST00000269305.8:c.-94C>T (TP53) | ENSP00000269305.4:n.-94C>T | |
| ENST00000316024.9:c.-1207G>A (WRAP53) | ENSP00000324203.5:n.-1207G>A | |
| ENST00000420246.6:c.-94C>T (TP53) | ENSP00000391127.2:n.-94C>T | |
| ENST00000431639.6:c.-1-1206G>A (WRAP53) | ENSP00000397219.2:n.-1-1206G>A | |
| ENST00000445888.6:c.-91C>T (TP53) | ENSP00000391478.2:n.-91C>T | |
| ENST00000455263.6:c.-94C>T (TP53) | ENSP00000398846.2:n.-94C>T | |
| ENST00000457584.6:c.-163G>A (WRAP53) | ENSP00000411061.2:n.-163G>A | |
| ENST00000505014.5:n.46C>T (TP53) | ||
| ENST00000509690.5:c.-87C>T (TP53) | ENSP00000425104.1:n.-87C>T | |
| ENST00000604348.5:c.-94C>T (TP53) | ENSP00000473895.1:n.-94C>T | |
| ENST00000610292.4:c.-328C>T (TP53) | ENSP00000478219.1:n.-328C>T | |
| ENST00000610538.4:c.-211C>T (TP53) | ENSP00000480868.1:n.-211C>T | |
| ENST00000617185.4:c.-94C>T (TP53) | ENSP00000482258.1:n.-94C>T | |
| ENST00000619485.4:c.-208C>T (TP53) | ENSP00000482537.1:n.-208C>T | |
| ENST00000620739.4:c.-211C>T (TP53) | ENSP00000481638.1:n.-211C>T | |
| ENST00000622645.4:c.-211C>T (TP53) | ENSP00000482222.1:n.-211C>T | |
| ENST00000635293.1:c.-211C>T (TP53) | ENSP00000488924.1:n.-211C>T | |
| NM_000546.5:c.-94C>T , LRG_321t1:c.-94C>T (TP53) | NP_000537.3:n.-94C>T | |
| NM_001126112.2:c.-91C>T , LRG_321t2:c.-91C>T (TP53) | NP_001119584.1:n.-91C>T | |
| NM_001126113.2:c.-94C>T , LRG_321t4:c.-94C>T (TP53) | NP_001119585.1:n.-94C>T | |
| NM_001126114.2:c.-94C>T , LRG_321t3:c.-94C>T (TP53) | NP_001119586.1:n.-94C>T | |
| NM_001126118.1:c.-328C>T , LRG_321t8:c.-328C>T (TP53) | NP_001119590.1:n.-328C>T | |
| NM_001143990.1:c.-1-1206G>A (WRAP53) | NP_001137462.1:n.-1-1206G>A | |
| NM_001143991.1:c.-163G>A (WRAP53) | NP_001137463.1:n.-163G>A | |
| NM_001276695.1:c.-211C>T (TP53) | NP_001263624.1:n.-211C>T | |
| NM_001276696.1:c.-211C>T (TP53) | NP_001263625.1:n.-211C>T | |
| NM_001276760.1:c.-211C>T (TP53) | NP_001263689.1:n.-211C>T | |
| NM_001276761.1:c.-208C>T (TP53) | NP_001263690.1:n.-208C>T | |
| NM_001143991.2:c.-163G>A (WRAP53) | NP_001137463.1:n.-163G>A | |
| NM_001276695.2:c.-211C>T (TP53) | NP_001263624.1:n.-211C>T | |
| NM_001276696.2:c.-211C>T (TP53) | NP_001263625.1:n.-211C>T | |
| NM_001276760.2:c.-211C>T (TP53) | NP_001263689.1:n.-211C>T | |
| NM_001276761.2:c.-208C>T (TP53) | NP_001263690.1:n.-208C>T | |
| NM_000546.6:c.-94C>T (TP53) MANE Select | NP_000537.3:n.-94C>T | |
| NM_001126112.3:c.-91C>T (TP53) | NP_001119584.1:n.-91C>T | |
| NM_001126113.3:c.-94C>T (TP53) | NP_001119585.1:n.-94C>T | |
| NM_001126114.3:c.-94C>T (TP53) | NP_001119586.1:n.-94C>T | |
| NM_001126118.2:c.-328C>T (TP53) | NP_001119590.1:n.-328C>T | |
| NM_001143990.2:c.-1-1206G>A (WRAP53) | NP_001137462.1:n.-1-1206G>A | |
| NM_001276695.3:c.-211C>T (TP53) | NP_001263624.1:n.-211C>T | |
| NM_001276696.3:c.-211C>T (TP53) | NP_001263625.1:n.-211C>T | |
| NM_001276760.3:c.-211C>T (TP53) | NP_001263689.1:n.-211C>T | |
| NM_001276761.3:c.-208C>T (TP53) | NP_001263690.1:n.-208C>T |