Linked Data
ClinVar Variation Id:
251884
ClinVar RCV Id:
RCV000237948
dbSNP Id:
rs879254930
PubMed:
PMID:11668627
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11113698delinsCTGAAT , CM000681.2:g.11113698delinsCTGAAT | GRCh38 |
| NC_000019.9:g.11224374delinsCTGAAT , CM000681.1:g.11224374delinsCTGAAT | GRCh37 |
| NC_000019.8:g.11085374delinsCTGAAT | NCBI36 |
| NG_009060.1:g.29318delinsCTGAAT , LRG_274:g.29318delinsCTGAAT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.1780delinsCTGAAT | ENSP00000252444.6:p.Arg594LeufsTer? | |
| ENST00000559340.2:c.1522delinsCTGAAT | ENSP00000453696.2:p.Arg508LeufsTer? | |
| ENST00000560467.2:c.1402delinsCTGAAT | ENSP00000453513.2:p.Arg468LeufsTer? | |
| ENST00000558518.6:c.1522delinsCTGAAT MANE Select | ENSP00000454071.1:p.Arg508LeufsTer? | |
| ENST00000252444.9:c.1776delinsCTGAAT | ||
| ENST00000455727.6:c.1018delinsCTGAAT | ENSP00000397829.2:p.Arg340LeufsTer? | |
| ENST00000535915.5:c.1399delinsCTGAAT | ENSP00000440520.1:p.Arg467LeufsTer? | |
| ENST00000545707.5:c.1141delinsCTGAAT | ENSP00000437639.1:p.Arg381LeufsTer? | |
| ENST00000557933.5:c.1522delinsCTGAAT | ENSP00000453557.1:p.Arg508LeufsTer? | |
| ENST00000558013.5:c.1522delinsCTGAAT | ENSP00000453346.1:p.Arg508LeufsTer? | |
| ENST00000558518.5:c.1522delinsCTGAAT | ENSP00000454071.1:p.Arg508LeufsTer? | |
| ENST00000559340.1:c.243delinsCTGAAT | ||
| NM_000527.4:c.1522delinsCTGAAT , LRG_274t1:c.1522delinsCTGAAT | NP_000518.1:p.Arg508LeufsTer? | |
| NM_001195798.1:c.1522delinsCTGAAT | NP_001182727.1:p.Arg508LeufsTer? | |
| NM_001195799.1:c.1399delinsCTGAAT | NP_001182728.1:p.Arg467LeufsTer? | |
| NM_001195800.1:c.1018delinsCTGAAT | NP_001182729.1:p.Arg340LeufsTer? | |
| NM_001195803.1:c.1141delinsCTGAAT | NP_001182732.1:p.Arg381LeufsTer? | |
| XM_011528010.1:c.1522delinsCTGAAT | XP_011526312.1:p.Arg508LeufsTer? | |
| XM_011528011.1:c.1141delinsCTGAAT | XP_011526313.1:p.Arg381LeufsTer? | |
| XR_244074.2:n.1672delinsCTGAAT | ||
| XM_011528010.2:c.1522delinsCTGAAT | XP_011526312.1:p.Arg508LeufsTer? | |
| XR_001753685.2:n.1639delinsCTGAAT | ||
| XR_001753686.2:n.1639delinsCTGAAT | ||
| NM_000527.5:c.1522delinsCTGAAT MANE Select | NP_000518.1:p.Arg508LeufsTer? | |
| NM_001195798.2:c.1522delinsCTGAAT | NP_001182727.1:p.Arg508LeufsTer? | |
| NM_001195799.2:c.1399delinsCTGAAT | NP_001182728.1:p.Arg467LeufsTer? | |
| NM_001195800.2:c.1018delinsCTGAAT | NP_001182729.1:p.Arg340LeufsTer? | |
| NM_001195803.2:c.1141delinsCTGAAT | NP_001182732.1:p.Arg381LeufsTer? |