Linked Data
ClinVar Variation Id:
919905
dbSNP Id:
rs754328605
ExAC:
19:11238687 T / C
gnomAD v2:
19-11238687-T-C
gnomAD v4:
19-11128011-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11128011T>C , CM000681.2:g.11128011T>C | GRCh38 |
| NC_000019.9:g.11238687T>C , CM000681.1:g.11238687T>C | GRCh37 |
| NC_000019.8:g.11099687T>C | NCBI36 |
| NG_009060.1:g.43631T>C , LRG_274:g.43631T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.2573T>C | ENSP00000252444.6:p.Leu858Pro | |
| ENST00000559340.2:c.*384T>C | ENSP00000453696.2:n.*384T>C | |
| ENST00000560467.2:c.2195T>C | ENSP00000453513.2:p.Leu732Pro | |
| ENST00000558518.6:c.2315T>C MANE Select | ENSP00000454071.1:p.Leu772Pro | |
| ENST00000252444.9:c.2569T>C | ||
| ENST00000455727.6:c.1811T>C | ENSP00000397829.2:p.Leu604Pro | |
| ENST00000535915.5:c.2192T>C | ENSP00000440520.1:p.Leu731Pro | |
| ENST00000545707.5:c.1781T>C | ENSP00000437639.1:p.Leu594Pro | |
| ENST00000557933.5:c.2315T>C | ENSP00000453557.1:p.Leu772Pro | |
| ENST00000558013.5:c.2315T>C | ENSP00000453346.1:p.Leu772Pro | |
| ENST00000558518.5:c.2315T>C | ENSP00000454071.1:p.Leu772Pro | |
| ENST00000560628.1:n.108+357T>C | ||
| NM_000527.4:c.2315T>C , LRG_274t1:c.2315T>C | NP_000518.1:p.Leu772Pro | |
| NM_001195798.1:c.2315T>C | NP_001182727.1:p.Leu772Pro | |
| NM_001195799.1:c.2192T>C | NP_001182728.1:p.Leu731Pro | |
| NM_001195800.1:c.1811T>C | NP_001182729.1:p.Leu604Pro | |
| NM_001195803.1:c.1781T>C | NP_001182732.1:p.Leu594Pro | |
| XM_011528010.1:c.2312-1502T>C | XP_011526312.1:n.2312-1502T>C | |
| XM_011528011.1:c.1934T>C | XP_011526313.1:p.Leu645Pro | |
| XR_244074.2:n.2325T>C | ||
| XM_011528010.2:c.2312-1502T>C | XP_011526312.1:n.2312-1502T>C | |
| XR_001753685.2:n.2649T>C | ||
| XR_001753686.2:n.2292T>C | ||
| NM_000527.5:c.2315T>C MANE Select | NP_000518.1:p.Leu772Pro | |
| NM_001195798.2:c.2315T>C | NP_001182727.1:p.Leu772Pro | |
| NM_001195799.2:c.2192T>C | NP_001182728.1:p.Leu731Pro | |
| NM_001195800.2:c.1811T>C | NP_001182729.1:p.Leu604Pro | |
| NM_001195803.2:c.1781T>C | NP_001182732.1:p.Leu594Pro |