Linked Data
ClinVar Variation Id:
491464
dbSNP Id:
rs587780830
gnomAD v2:
17-59761132-G-T
gnomAD v4:
17-61683771-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.61683771G>T , CM000679.2:g.61683771G>T | GRCh38 |
| NC_000017.10:g.59761132G>T , CM000679.1:g.59761132G>T | GRCh37 |
| NC_000017.9:g.57115914G>T | NCBI36 |
| NG_007409.2:g.184789C>A , LRG_300:g.184789C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682073.1:n.2015C>A | ||
| ENST00000682453.1:c.3275C>A | ENSP00000506943.1:p.Pro1092Gln | |
| ENST00000682477.1:c.*2701C>A | ENSP00000507075.1:n.*2701C>A | |
| ENST00000682589.1:n.9152C>A | ||
| ENST00000682755.1:c.3053C>A | ENSP00000507660.1:p.Pro1018Gln | |
| ENST00000682989.1:c.*366C>A | ENSP00000507786.1:n.*366C>A | |
| ENST00000683039.1:c.3275C>A | ENSP00000508303.1:p.Pro1092Gln | |
| ENST00000683235.1:c.*690C>A | ENSP00000507646.1:n.*690C>A | |
| ENST00000683535.1:n.1405C>A | ||
| ENST00000684584.1:c.2438C>A | ENSP00000508044.1:p.Pro813Gln | |
| ENST00000684626.1:n.1521C>A | ||
| ENST00000684769.1:c.1465C>A | ENSP00000507691.1:n.1465C>A | |
| ENST00000259008.7:c.3275C>A MANE Select | ENSP00000259008.2:p.Pro1092Gln | |
| ENST00000259008.6:c.3275C>A | ENSP00000259008.2:p.Pro1092Gln | |
| NM_032043.2:c.3275C>A , LRG_300t1:c.3275C>A | NP_114432.2:p.Pro1092Gln | |
| XM_011525332.1:c.3335C>A | XP_011523634.1:p.Pro1112Gln | |
| XM_011525333.1:c.3335C>A | XP_011523635.1:p.Pro1112Gln | |
| XM_011525334.1:c.3335C>A | XP_011523636.1:p.Pro1112Gln | |
| XM_011525335.1:c.3275C>A | XP_011523637.1:p.Pro1092Gln | |
| XM_011525336.1:c.3215C>A | XP_011523638.1:p.Pro1072Gln | |
| XM_011525337.1:c.3134C>A | XP_011523639.1:p.Pro1045Gln | |
| XM_011525338.1:c.2852C>A | XP_011523640.1:p.Pro951Gln | |
| XM_011525332.3:c.3335C>A | XP_011523634.1:p.Pro1112Gln | |
| XM_011525333.3:c.3335C>A | XP_011523635.1:p.Pro1112Gln | |
| XM_011525334.2:c.3335C>A | XP_011523636.1:p.Pro1112Gln | |
| XM_011525335.3:c.3275C>A | XP_011523637.1:p.Pro1092Gln | |
| XM_011525336.2:c.3215C>A | XP_011523638.1:p.Pro1072Gln | |
| XM_011525337.2:c.3134C>A | XP_011523639.1:p.Pro1045Gln | |
| XM_011525338.2:c.2852C>A | XP_011523640.1:p.Pro951Gln | |
| XM_017025200.1:c.2792C>A | XP_016880689.1:p.Pro931Gln | |
| XM_017025201.1:c.2792C>A | XP_016880690.1:p.Pro931Gln | |
| XM_017025202.1:c.1421C>A | XP_016880691.1:p.Pro474Gln | |
| XM_017025203.1:c.1421C>A | XP_016880692.1:p.Pro474Gln | |
| NM_032043.3:c.3275C>A MANE Select | NP_114432.2:p.Pro1092Gln |