Revel Score:
ENST00000412955
0.639
ENST00000320741 (MANE Select)
0.639
ENST00000444204
0.639
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.186854303C>G , CM000665.2:g.186854303C>G | GRCh38 |
| NC_000003.11:g.186572092C>G , CM000665.1:g.186572092C>G | GRCh37 |
| NC_000003.10:g.188054786C>G | NCBI36 |
| NG_021140.1:g.16630C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320741.7:c.334C>G (ADIPOQ) MANE Select | ENSP00000320709.2:p.Arg112Gly | |
| ENST00000320741.6:c.334C>G (ADIPOQ) | ENSP00000320709.2:p.Arg112Gly | |
| ENST00000444204.2:c.334C>G (ADIPOQ) | ENSP00000389814.2:p.Arg112Gly | |
| NM_001177800.1:c.334C>G (ADIPOQ) | NP_001171271.1:p.Arg112Gly | |
| NM_004797.3:c.334C>G (ADIPOQ) | NP_004788.1:p.Arg112Gly | |
| NR_046662.1:n.1821G>C (ADIPOQ-AS1) | ||
| XM_011513324.1:c.334C>G (ADIPOQ) | XP_011511626.1:p.Arg112Gly | |
| NR_046662.2:n.1950G>C (ADIPOQ-AS1) | ||
| NM_004797.4:c.334C>G (ADIPOQ) MANE Select | NP_004788.1:p.Arg112Gly | |
| NM_001177800.2:c.334C>G (ADIPOQ) | NP_001171271.1:p.Arg112Gly |