ClinVar Variation:
dbSNP:
gnomAD v2:
gnomAD v3:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.160307686C>T , CM000665.2:g.160307686C>T | GRCh38 |
| NC_000003.11:g.160025474C>T , CM000665.1:g.160025474C>T | GRCh37 |
| NC_000003.10:g.161508168C>T | NCBI36 |
| NG_022932.1:g.96847G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326448.12:c.1053G>A (IFT80) MANE Select | ENSP00000312778.7:p.Thr351= | |
| ENST00000326448.11:c.1053G>A (IFT80) | ENSP00000312778.7:p.Thr351= | |
| ENST00000461213.1:n.484G>A (IFT80) | ||
| ENST00000472555.5:c.590G>A (IFT80) | ||
| ENST00000483325.1:c.96G>A (IFT80) | ENSP00000417552.1:p.Thr32= | |
| ENST00000483465.5:c.642G>A (IFT80) | ENSP00000418196.1:p.Thr214= | |
| ENST00000483754.1:c.1566G>A (TRIM59-IFT80) | ENSP00000456272.1:p.Thr522= | |
| ENST00000487943.5:n.2272G>A (IFT80) | ||
| ENST00000496589.5:c.642G>A (IFT80) | ENSP00000420646.1:p.Thr214= | |
| NM_001190241.1:c.642G>A (IFT80) | NP_001177170.1:p.Thr214= | |
| NM_001190242.1:c.642G>A (IFT80) | NP_001177171.1:p.Thr214= | |
| NM_020800.2:c.1053G>A (IFT80) | NP_065851.1:p.Thr351= | |
| NR_148401.1:n.1761G>A (TRIM59-IFT80) | ||
| NR_148402.1:n.3297G>A (TRIM59-IFT80) | ||
| NR_148403.1:n.3564G>A (TRIM59-IFT80) | ||
| NM_020800.3:c.1053G>A (IFT80) MANE Select | NP_065851.1:p.Thr351= | |
| NM_001190241.2:c.642G>A (IFT80) | NP_001177170.1:p.Thr214= | |
| NM_001190242.2:c.642G>A (IFT80) | NP_001177171.1:p.Thr214= |