Linked Data
ClinVar Variation Id:
251378
ClinVar RCV Id:
RCV000237202
dbSNP Id:
rs879254631
MyVariant Identifiers:
chr19:g.11216255_11216264delinsTGCAA (hg19)
chr19:g.11105579_11105588delinsTGCAA (hg38)
PubMed:
PMID:20809525
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11105579_11105588delinsTGCAA , CM000681.2:g.11105579_11105588delinsTGCAA | GRCh38 |
| NC_000019.9:g.11216255_11216264delinsTGCAA , CM000681.1:g.11216255_11216264delinsTGCAA | GRCh37 |
| NC_000019.8:g.11077255_11077264delinsTGCAA | NCBI36 |
| NG_009060.1:g.21199_21208delinsTGCAA , LRG_274:g.21199_21208delinsTGCAA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.931_940delinsTGCAA | ENSP00000252444.6:p.Lys311CysfsTer13 | |
| ENST00000559340.2:c.673_682delinsTGCAA | ENSP00000453696.2:p.Lys225CysfsTer13 | |
| ENST00000560467.2:c.673_682delinsTGCAA | ENSP00000453513.2:p.Lys225CysfsTer13 | |
| ENST00000558518.6:c.673_682delinsTGCAA MANE Select | ENSP00000454071.1:p.Lys225CysfsTer13 | |
| ENST00000252444.9:c.927_936delinsTGCAA | ||
| ENST00000455727.6:c.314-1813_314-1804delinsTGCAA | ENSP00000397829.2:n.314-1813_314-1804delinsTGCAA | |
| ENST00000535915.5:c.550_559delinsTGCAA | ENSP00000440520.1:p.Lys184CysfsTer13 | |
| ENST00000545707.5:c.314-986_314-977delinsTGCAA | ENSP00000437639.1:n.314-986_314-977delinsTGCAA | |
| ENST00000557933.5:c.673_682delinsTGCAA | ENSP00000453557.1:p.Lys225CysfsTer13 | |
| ENST00000558013.5:c.673_682delinsTGCAA | ENSP00000453346.1:p.Lys225CysfsTer13 | |
| ENST00000558518.5:c.673_682delinsTGCAA | ENSP00000454071.1:p.Lys225CysfsTer13 | |
| ENST00000560467.1:c.273_282delinsTGCAA | ||
| NM_000527.4:c.673_682delinsTGCAA , LRG_274t1:c.673_682delinsTGCAA | NP_000518.1:p.Lys225CysfsTer13 | |
| NM_001195798.1:c.673_682delinsTGCAA | NP_001182727.1:p.Lys225CysfsTer13 | |
| NM_001195799.1:c.550_559delinsTGCAA | NP_001182728.1:p.Lys184CysfsTer13 | |
| NM_001195800.1:c.314-1813_314-1804delinsTGCAA | NP_001182729.1:n.314-1813_314-1804delinsTGCAA | |
| NM_001195803.1:c.314-986_314-977delinsTGCAA | NP_001182732.1:n.314-986_314-977delinsTGCAA | |
| XM_011528010.1:c.673_682delinsTGCAA | XP_011526312.1:p.Lys225CysfsTer13 | |
| XM_011528011.1:c.314-986_314-977delinsTGCAA | XP_011526313.1:n.314-986_314-977delinsTGCAA | |
| XR_244074.2:n.823_832delinsTGCAA | ||
| XM_011528010.2:c.673_682delinsTGCAA | XP_011526312.1:p.Lys225CysfsTer13 | |
| XR_001753685.2:n.790_799delinsTGCAA | ||
| XR_001753686.2:n.790_799delinsTGCAA | ||
| NM_000527.5:c.673_682delinsTGCAA MANE Select | NP_000518.1:p.Lys225CysfsTer13 | |
| NM_001195798.2:c.673_682delinsTGCAA | NP_001182727.1:p.Lys225CysfsTer13 | |
| NM_001195799.2:c.550_559delinsTGCAA | NP_001182728.1:p.Lys184CysfsTer13 | |
| NM_001195800.2:c.314-1813_314-1804delinsTGCAA | NP_001182729.1:n.314-1813_314-1804delinsTGCAA | |
| NM_001195803.2:c.314-986_314-977delinsTGCAA | NP_001182732.1:n.314-986_314-977delinsTGCAA |