Linked Data
dbSNP Id:
rs1453843217
gnomAD v2:
12-8757831-AT-A
gnomAD v3:
12-8605235-AT-A
gnomAD v4:
12-8605235-AT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.8605238del , CM000674.2:g.8605238del | GRCh38 |
| NC_000012.11:g.8757834del , CM000674.1:g.8757834del | GRCh37 |
| NC_000012.10:g.8649101del | NCBI36 |
| NG_011588.1:g.12611del , LRG_17:g.12611del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000537228.6:c.406del | ENSP00000445691.1:p.Ile136Ter | |
| ENST00000543081.6:c.406del | ENSP00000439103.2:p.Ile136Ter | |
| ENST00000544516.6:c.157-899del | ENSP00000439538.2:n.157-899del | |
| ENST00000545576.2:n.515del | ||
| ENST00000696246.1:c.391del | ENSP00000512504.1:p.Ile131Ter | |
| ENST00000696271.1:n.526del | ||
| ENST00000696272.1:c.391del | ENSP00000512515.1:p.Ile131Ter | |
| ENST00000696273.1:c.439del | ENSP00000512516.1:p.Ile147Ter | |
| ENST00000229335.11:c.406del MANE Select | ENSP00000229335.6:p.Ile136Ter | |
| ENST00000229335.10:c.406del | ENSP00000229335.6:p.Ile136Ter | |
| ENST00000537228.5:c.406del | ENSP00000445691.1:p.Ile136Ter | |
| ENST00000543081.5:c.402del | ||
| ENST00000544516.5:c.153-899del | ||
| ENST00000545512.1:c.402del | ||
| ENST00000545576.1:n.440del | ||
| NM_020661.2:c.406del , LRG_17t1:c.406del | NP_065712.1:p.Ile136Ter | |
| XM_011520772.1:c.406del | XP_011519074.1:p.Ile136Ter | |
| XM_011520773.1:c.406del | XP_011519075.1:p.Ile136Ter | |
| NM_001330343.1:c.406del | NP_001317272.1:p.Ile136Ter | |
| NM_020661.3:c.406del | NP_065712.1:p.Ile136Ter | |
| XM_011520773.2:c.406del | XP_011519075.1:p.Ile136Ter | |
| NM_020661.4:c.406del MANE Select | NP_065712.1:p.Ile136Ter | |
| NM_001330343.2:c.406del | NP_001317272.1:p.Ile136Ter |