Linked Data
ClinVar Variation Id:
534388
dbSNP Id:
rs1187396214
gnomAD v3:
6-133512971-G-T
gnomAD v4:
6-133512971-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.133512971G>T , CM000668.2:g.133512971G>T | GRCh38 |
| NC_000006.11:g.133834109G>T , CM000668.1:g.133834109G>T | GRCh37 |
| NC_000006.10:g.133875802G>T | NCBI36 |
| NG_011596.1:g.276615G>T | |
| NG_011596.2:g.276615G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000525849.7:c.1365G>T (EYA4) | ENSP00000433219.1:p.Met455Ile | |
| ENST00000706301.1:c.1272G>T (EYA4) | ENSP00000516341.1:p.Met424Ile | |
| ENST00000355167.8:c.1290G>T (EYA4) | ENSP00000347294.4:p.Met430Ile | |
| ENST00000683325.1:c.*7G>T (EYA4) | ENSP00000508141.1:n.*7G>T | |
| ENST00000683674.1:n.335G>T (EYA4) | ||
| ENST00000684773.1:c.957G>T (EYA4) | ENSP00000506812.1:p.Met319Ile | |
| ENST00000355286.12:c.1434G>T (EYA4) MANE Select | ENSP00000347434.7:p.Met478Ile | |
| ENST00000431403.3:c.1365G>T (EYA4) | ENSP00000404558.3:p.Met455Ile | |
| ENST00000525849.6:c.1365G>T (EYA4) | ENSP00000433219.1:p.Met455Ile | |
| ENST00000355167.7:c.1434G>T (EYA4) | ENSP00000347294.3:p.Met478Ile | |
| ENST00000355286.10:c.1365G>T (EYA4) | ENSP00000347434.6:p.Met455Ile | |
| ENST00000367895.9:c.1434G>T (EYA4) | ENSP00000356870.5:p.Met478Ile | |
| ENST00000430974.6:c.1290G>T (EYA4) | ENSP00000388670.2:p.Met430Ile | |
| ENST00000431403.2:c.1434G>T (EYA4) | ENSP00000404558.2:p.Met478Ile | |
| ENST00000452339.6:c.1272G>T (EYA4) | ENSP00000395916.2:p.Met424Ile | |
| ENST00000525849.5:c.1365G>T (EYA4) | ENSP00000433219.1:p.Met455Ile | |
| ENST00000531901.5:c.1452G>T (EYA4) | ENSP00000432770.1:p.Met484Ile | |
| ENST00000532518.1:n.712G>T (EYA4) | ||
| NM_001301012.1:c.1272G>T (EYA4) | NP_001287941.1:p.Met424Ile | |
| NM_001301013.1:c.1452G>T (EYA4) | NP_001287942.1:p.Met484Ile | |
| NM_004100.4:c.1434G>T (EYA4) | NP_004091.3:p.Met478Ile | |
| NM_172103.3:c.1365G>T (EYA4) | NP_742101.2:p.Met455Ile | |
| NM_172105.3:c.1434G>T (EYA4) | NP_742103.1:p.Met478Ile | |
| NR_109982.1:n.2286-5650C>A (TARID) | ||
| XM_005266851.3:c.1452G>T (EYA4) | XP_005266908.1:p.Met484Ile | |
| XM_005266852.3:c.1452G>T (EYA4) | XP_005266909.1:p.Met484Ile | |
| XM_005266853.3:c.1365G>T (EYA4) | XP_005266910.1:p.Met455Ile | |
| XM_011535540.1:c.1383G>T (EYA4) | XP_011533842.1:p.Met461Ile | |
| XM_011535541.1:c.1368G>T (EYA4) | XP_011533843.1:p.Met456Ile | |
| XM_011535542.1:c.1290G>T (EYA4) | XP_011533844.1:p.Met430Ile | |
| XM_005266851.5:c.1452G>T (EYA4) | XP_005266908.1:p.Met484Ile | |
| XM_005266853.5:c.1365G>T (EYA4) | XP_005266910.1:p.Met455Ile | |
| XM_017010368.2:c.1452G>T (EYA4) | XP_016865857.1:p.Met484Ile | |
| XM_017010369.2:c.1434G>T (EYA4) | XP_016865858.1:p.Met478Ile | |
| XM_017010370.2:c.1383G>T (EYA4) | XP_016865859.1:p.Met461Ile | |
| XM_017010371.2:c.1368G>T (EYA4) | XP_016865860.1:p.Met456Ile | |
| XM_017010372.2:c.1290G>T (EYA4) | XP_016865861.1:p.Met430Ile | |
| XM_017010373.2:c.1272G>T (EYA4) | XP_016865862.1:p.Met424Ile | |
| XM_017010374.2:c.1290G>T (EYA4) | XP_016865863.1:p.Met430Ile | |
| XM_017010375.1:c.1290G>T (EYA4) | XP_016865864.1:p.Met430Ile | |
| XR_001743219.2:n.1546G>T (EYA4) | ||
| XR_001743220.2:n.1528G>T (EYA4) | ||
| NM_004100.5:c.1434G>T (EYA4) MANE Select | NP_004091.3:p.Met478Ile | |
| NM_001370458.1:c.1365G>T (EYA4) | NP_001357387.1:p.Met455Ile | |
| NM_001370459.1:c.1290G>T (EYA4) | NP_001357388.1:p.Met430Ile | |
| NM_001301012.2:c.1272G>T (EYA4) | NP_001287941.1:p.Met424Ile | |
| NM_001301013.2:c.1452G>T (EYA4) | NP_001287942.1:p.Met484Ile | |
| NM_172103.4:c.1365G>T (EYA4) | NP_742101.2:p.Met455Ile | |
| NM_172105.4:c.1434G>T (EYA4) | NP_742103.1:p.Met478Ile |