Linked Data
ClinVar Variation Id:
378892
ClinVar RCV Id:
RCV000421387
dbSNP Id:
rs1020264217
gnomAD v4:
6-145735178-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.145735178C>A , CM000668.2:g.145735178C>A | GRCh38 |
| NC_000006.11:g.146056314C>A , CM000668.1:g.146056314C>A | GRCh37 |
| NC_000006.10:g.146098007C>A | NCBI36 |
| NG_012832.1:g.5678G>T | |
| NG_012832.2:g.5678G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367519.9:c.301+20G>T (EPM2A) MANE Select | ENSP00000356489.3:n.301+20G>T | |
| ENST00000435470.2:c.301+20G>T (EPM2A) | ENSP00000405913.2:n.301+20G>T | |
| ENST00000611340.5:c.-114+818G>T (EPM2A) | ENSP00000480268.1:n.-114+818G>T | |
| ENST00000638262.1:c.301+20G>T (EPM2A) | ENSP00000492876.1:n.301+20G>T | |
| ENST00000638554.1:c.79+20G>T (EPM2A) | ENSP00000492823.1:n.79+20G>T | |
| ENST00000638717.1:c.84+20G>T (EPM2A) | ||
| ENST00000639049.1:c.273+20G>T (EPM2A) | ||
| ENST00000639423.1:c.-114+730G>T (EPM2A) | ENSP00000492701.1:n.-114+730G>T | |
| ENST00000639649.1:n.249G>T (EPM2A) | ||
| ENST00000640297.1:n.317+20G>T (EPM2A) | ||
| ENST00000640351.1:c.37+67G>T (EPM2A) | ||
| ENST00000640898.1:n.82+730G>T (EPM2A) | ||
| ENST00000640980.1:c.-114+730G>T (EPM2A) | ENSP00000491191.1:n.-114+730G>T | |
| ENST00000367519.7:c.301+20G>T (EPM2A) | ENSP00000356489.3:n.301+20G>T | |
| ENST00000435470.1:c.60+20G>T (EPM2A) | ||
| ENST00000618445.4:c.301+20G>T (EPM2A) | ENSP00000480339.1:n.301+20G>T | |
| NM_001018041.1:c.301+20G>T (EPM2A) | NP_001018051.1:n.301+20G>T | |
| NM_005670.3:c.301+20G>T (EPM2A) | NP_005661.1:n.301+20G>T | |
| NR_038246.1:n.52+258C>A (EPM2A-DT) | ||
| XM_006715564.2:c.301+20G>T (EPM2A) | XP_006715627.1:n.301+20G>T | |
| XM_011536113.1:c.301+20G>T (EPM2A) | XP_011534415.1:n.301+20G>T | |
| XM_011536114.1:c.301+20G>T (EPM2A) | XP_011534416.1:n.301+20G>T | |
| XM_011536115.1:c.301+20G>T (EPM2A) | XP_011534417.1:n.301+20G>T | |
| NM_001360057.1:c.301+20G>T (EPM2A) | NP_001346986.1:n.301+20G>T | |
| NM_001360064.1:c.-114+730G>T (EPM2A) | NP_001346993.1:n.-114+730G>T | |
| NM_001360071.1:c.-369+20G>T (EPM2A) | NP_001347000.1:n.-369+20G>T | |
| NR_153397.1:n.323+20G>T (EPM2A) | ||
| NR_153398.1:n.114+730G>T (EPM2A) | ||
| XM_011536113.2:c.301+20G>T (EPM2A) | XP_011534415.1:n.301+20G>T | |
| XM_024446550.1:c.301+20G>T (EPM2A) | XP_024302318.1:n.301+20G>T | |
| NM_005670.4:c.301+20G>T (EPM2A) MANE Select | NP_005661.1:n.301+20G>T | |
| NM_001018041.2:c.301+20G>T (EPM2A) | NP_001018051.1:n.301+20G>T | |
| NM_001360057.2:c.301+20G>T (EPM2A) | NP_001346986.1:n.301+20G>T | |
| NM_001360064.2:c.-114+730G>T (EPM2A) | NP_001346993.1:n.-114+730G>T | |
| NM_001360071.2:c.-369+20G>T (EPM2A) | NP_001347000.1:n.-369+20G>T | |
| NM_001368129.2:c.-323+20G>T (EPM2A) | NP_001355058.1:n.-323+20G>T | |
| NM_001368130.1:c.301+20G>T (EPM2A) | NP_001355059.1:n.301+20G>T | |
| NM_001368131.1:c.-114+67G>T (EPM2A) | NP_001355060.1:n.-114+67G>T | |
| NR_153398.2:n.116+730G>T (EPM2A) |