Linked Data
ClinVar Variation Id:
554096
dbSNP Id:
rs1555598869
gnomAD v4:
17-80105022-AT-A
MyVariant Identifiers:
chr17:g.80105023del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.80105023del , CM000679.2:g.80105023del | GRCh38 |
| NC_000017.10:g.78078822del , CM000679.1:g.78078822del | GRCh37 |
| NC_000017.9:g.75693417del | NCBI36 |
| NG_009822.1:g.8468del , LRG_673:g.8468del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000570803.6:c.437del | ENSP00000460543.2:p.Met146ArgfsTer7 | |
| ENST00000572080.2:c.437del | ENSP00000459972.2:p.Met146ArgfsTer7 | |
| ENST00000577106.6:c.437del | ENSP00000458306.2:p.Met146ArgfsTer7 | |
| ENST00000302262.8:c.437del MANE Select | ENSP00000305692.3:p.Met146ArgfsTer7 | |
| ENST00000302262.7:c.437del | ENSP00000305692.3:p.Met146ArgfsTer7 | |
| ENST00000390015.7:c.437del | ENSP00000374665.3:p.Met146ArgfsTer7 | |
| ENST00000570803.5:c.437del | ENSP00000460543.1:p.Met146ArgfsTer7 | |
| ENST00000577106.5:c.437del | ENSP00000458306.1:p.Met146ArgfsTer7 | |
| NM_000152.3:c.437del , LRG_673t1:c.437del | NP_000143.2:p.Met146ArgfsTer7 | |
| NM_001079803.1:c.437del | NP_001073271.1:p.Met146ArgfsTer7 | |
| NM_001079804.1:c.437del | NP_001073272.1:p.Met146ArgfsTer7 | |
| XM_005257193.1:c.437del | XP_005257250.1:p.Met146ArgfsTer7 | |
| XM_005257194.3:c.437del | XP_005257251.1:p.Met146ArgfsTer7 | |
| NM_000152.4:c.437del | NP_000143.2:p.Met146ArgfsTer7 | |
| NM_001079803.2:c.437del | NP_001073271.1:p.Met146ArgfsTer7 | |
| NM_001079804.2:c.437del | NP_001073272.1:p.Met146ArgfsTer7 | |
| XM_005257193.2:c.437del | XP_005257250.1:p.Met146ArgfsTer7 | |
| XM_005257194.4:c.437del | XP_005257251.1:p.Met146ArgfsTer7 | |
| NM_000152.5:c.437del MANE Select | NP_000143.2:p.Met146ArgfsTer7 | |
| NM_001079803.3:c.437del | NP_001073271.1:p.Met146ArgfsTer7 | |
| NM_001079804.3:c.437del | NP_001073272.1:p.Met146ArgfsTer7 |