Linked Data
gnomAD v2:
19-11533534-GGGC-G
gnomAD v4:
19-11422866-GGGC-G
MyVariant Identifiers:
chr19:g.11533535_11533537del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11422867_11422869del , CM000681.2:g.11422867_11422869del | GRCh38 |
| NC_000019.9:g.11533535_11533537del , CM000681.1:g.11533535_11533537del | GRCh37 |
| NC_000019.8:g.11394535_11394537del | NCBI36 |
| NG_041777.1:g.17914_17916del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356392.9:c.1117-8_1117-6del MANE Select | ENSP00000348757.3:n.1117-8_1117-6del | |
| ENST00000356392.8:c.1117-8_1117-6del | ENSP00000348757.3:n.1117-8_1117-6del | |
| ENST00000586836.5:c.544-8_544-6del | ENSP00000467429.1:n.544-8_544-6del | |
| ENST00000591179.5:c.937-8_937-6del | ENSP00000466800.1:n.937-8_937-6del | |
| ENST00000591345.5:c.*1036-8_*1036-6del | ENSP00000467313.1:n.*1036-8_*1036-6del | |
| NM_001302453.1:c.955-8_955-6del | NP_001289382.1:n.955-8_955-6del | |
| NM_001302454.1:c.937-8_937-6del | NP_001289383.1:n.937-8_937-6del | |
| NM_145045.4:c.1117-8_1117-6del | NP_659482.3:n.1117-8_1117-6del | |
| XM_017026241.1:c.*11-8_*11-6del | XP_016881730.1:n.*11-8_*11-6del | |
| NM_145045.5:c.1117-8_1117-6del MANE Select | NP_659482.3:n.1117-8_1117-6del | |
| NM_001302454.2:c.937-8_937-6del | NP_001289383.1:n.937-8_937-6del |