dbSNP:
gnomAD v2:
gnomAD v3:
gnomAD v4:
Revel Score:
ENST00000390677 (MANE Select)
0.055
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.10908523T>A , CM000674.2:g.10908523T>A | GRCh38 |
| NC_000012.11:g.11061122T>A , CM000674.1:g.11061122T>A | GRCh37 |
| NC_000012.10:g.10952389T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703543.1:c.-58-24248A>T | ENSP00000515364.1:n.-58-24248A>T | |
| ENST00000535024.6:c.104-60116A>T | ENSP00000481571.2:n.104-60116A>T | |
| ENST00000390677.2:c.776A>T (TAS2R13) MANE Select | ENSP00000375095.2:p.Asn259Ile | |
| ENST00000535024.5:c.104-60116A>T (PRR4) | ENSP00000481571.1:n.104-60116A>T | |
| ENST00000536086.2:n.90-16598A>T (PRH1) | ||
| ENST00000536668.2:c.177-24248A>T | ENSP00000482961.1:n.177-24248A>T | |
| ENST00000539853.5:c.-58-24248A>T (PRH1) | ENSP00000482068.1:n.-58-24248A>T | |
| ENST00000541977.5:n.360-25427A>T (PRH1) | ||
| ENST00000546317.1:n.53-13194A>T (PRR4) | ||
| NM_001291314.1:c.-58-24248A>T (PRH1) | NP_001278243.1:n.-58-24248A>T | |
| NM_001291315.1:c.104-25427A>T (PRH1) | NP_001278244.1:n.104-25427A>T | |
| NM_023920.2:c.776A>T (TAS2R13) MANE Select | NP_076409.1:p.Asn259Ile | |
| NR_037918.2:n.545-24248A>T | ||
| NM_001291314.2:c.-58-24248A>T (PRH1) | NP_001278243.1:n.-58-24248A>T | |
| NM_001291315.2:c.104-25427A>T (PRH1) | NP_001278244.1:n.104-25427A>T |