Linked Data
ClinVar Variation Id:
1378661
ClinVar RCV Id:
RCV001914660
dbSNP Id:
rs2146205858
gnomAD v4:
22-18913529-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.18913529G>A , CM000684.2:g.18913529G>A | GRCh38 |
| NC_000022.10:g.18901042G>A , CM000684.1:g.18901042G>A | GRCh37 |
| NC_000022.9:g.17281042G>A | NCBI36 |
| NG_008226.2:g.28025C>T | |
| NG_009052.1:g.12307G>A | |
| NG_008226.3:g.28025C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357068.11:c.1527-3C>T (PRODH) MANE Select | ENSP00000349577.6:n.1527-3C>T | |
| ENST00000638240.1:c.513+2501G>A | ENSP00000492446.1:n.513+2501G>A | |
| ENST00000313755.9:n.2292-3C>T (PRODH) | ||
| ENST00000334029.6:c.1203-3C>T (PRODH) | ENSP00000334726.2:n.1203-3C>T | |
| ENST00000357068.10:c.1527-3C>T (PRODH) | ENSP00000349577.6:n.1527-3C>T | |
| ENST00000420436.5:c.1203-3C>T (PRODH) | ENSP00000410805.1:n.1203-3C>T | |
| ENST00000429300.5:n.1898-3C>T (PRODH) | ||
| ENST00000482858.5:n.4007-3C>T (PRODH) | ||
| ENST00000483718.5:c.*2171G>A (DGCR6) | ENSP00000467483.1:n.*2171G>A | |
| ENST00000491604.5:n.2436-3C>T (PRODH) | ||
| ENST00000610940.4:c.1527-3C>T (PRODH) | ENSP00000480347.1:n.1527-3C>T | |
| NM_001195226.1:c.1203-3C>T (PRODH) | NP_001182155.1:n.1203-3C>T | |
| NM_016335.4:c.1527-3C>T (PRODH) | NP_057419.4:n.1527-3C>T | |
| XM_011530278.1:c.954-3C>T (PRODH) | XP_011528580.1:n.954-3C>T | |
| XM_011530279.1:c.747-3C>T (PRODH) | XP_011528581.1:n.747-3C>T | |
| XR_937876.1:n.1594-3C>T (PRODH) | ||
| NM_005675.5:c.*1840G>A (DGCR6) | NP_005666.2:n.*1840G>A | |
| NM_001195226.2:c.1203-3C>T (PRODH) | NP_001182155.2:n.1203-3C>T | |
| NM_016335.5:c.1527-3C>T (PRODH) | NP_057419.5:n.1527-3C>T | |
| NM_016335.6:c.1527-3C>T (PRODH) MANE Select | NP_057419.5:n.1527-3C>T |