Linked Data
ClinVar Variation Id:
252327
dbSNP Id:
rs879255203
gnomAD v2:
19-11240210-T-C
gnomAD v3:
19-11129534-T-C
gnomAD v4:
19-11129534-T-C
PubMed:
PMID:16250003
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11129534T>C , CM000681.2:g.11129534T>C | GRCh38 |
| NC_000019.9:g.11240210T>C , CM000681.1:g.11240210T>C | GRCh37 |
| NC_000019.8:g.11101210T>C | NCBI36 |
| NG_009060.1:g.45154T>C , LRG_274:g.45154T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.2669T>C | ENSP00000252444.6:p.Leu890Pro | |
| ENST00000559340.2:c.*480T>C | ENSP00000453696.2:n.*480T>C | |
| ENST00000560467.2:c.2291T>C | ENSP00000453513.2:p.Leu764Pro | |
| ENST00000558518.6:c.2411T>C MANE Select | ENSP00000454071.1:p.Leu804Pro | |
| ENST00000252444.9:c.2665T>C | ||
| ENST00000455727.6:c.1907T>C | ENSP00000397829.2:p.Leu636Pro | |
| ENST00000535915.5:c.2288T>C | ENSP00000440520.1:p.Leu763Pro | |
| ENST00000545707.5:c.1877T>C | ENSP00000437639.1:p.Leu626Pro | |
| ENST00000557933.5:c.2473T>C | ENSP00000453557.1:p.Trp825Arg | |
| ENST00000558013.5:c.2411T>C | ENSP00000453346.1:p.Leu804Pro | |
| ENST00000558518.5:c.2411T>C | ENSP00000454071.1:p.Leu804Pro | |
| ENST00000560628.1:n.108+1880T>C | ||
| NM_000527.4:c.2411T>C , LRG_274t1:c.2411T>C | NP_000518.1:p.Leu804Pro | |
| NM_001195798.1:c.2411T>C | NP_001182727.1:p.Leu804Pro | |
| NM_001195799.1:c.2288T>C | NP_001182728.1:p.Leu763Pro | |
| NM_001195800.1:c.1907T>C | NP_001182729.1:p.Leu636Pro | |
| NM_001195803.1:c.1877T>C | NP_001182732.1:p.Leu626Pro | |
| XM_011528010.1:c.2333T>C | XP_011526312.1:p.Leu778Pro | |
| XM_011528011.1:c.2030T>C | XP_011526313.1:p.Leu677Pro | |
| XR_244074.2:n.2421T>C | ||
| XM_011528010.2:c.2333T>C | XP_011526312.1:p.Leu778Pro | |
| XR_001753685.2:n.2745T>C | ||
| XR_001753686.2:n.2388T>C | ||
| NM_000527.5:c.2411T>C MANE Select | NP_000518.1:p.Leu804Pro | |
| NM_001195798.2:c.2411T>C | NP_001182727.1:p.Leu804Pro | |
| NM_001195799.2:c.2288T>C | NP_001182728.1:p.Leu763Pro | |
| NM_001195800.2:c.1907T>C | NP_001182729.1:p.Leu636Pro | |
| NM_001195803.2:c.1877T>C | NP_001182732.1:p.Leu626Pro |