Linked Data
gnomAD v4:
9-136674860-AC-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.136674864del , CM000671.2:g.136674864del | GRCh38 |
| NC_000009.11:g.139569316del , CM000671.1:g.139569316del | GRCh37 |
| NC_000009.10:g.138689137del | NCBI36 |
| NG_008090.1:g.17599del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371696.7:c.589-54del MANE Select | ENSP00000360761.2:n.589-54del | |
| ENST00000371694.7:c.493-54del | ENSP00000360759.3:n.493-54del | |
| ENST00000371696.6:c.589-54del | ENSP00000360761.2:n.589-54del | |
| ENST00000472820.1:n.517-54del | ||
| ENST00000538402.1:c.589-54del | ENSP00000438919.1:n.589-54del | |
| NM_001012727.1:c.493-54del | NP_001012745.1:n.493-54del | |
| NM_006412.3:c.589-54del | NP_006403.2:n.589-54del | |
| NM_006412.4:c.589-54del MANE Select | NP_006403.2:n.589-54del | |
| NM_001012727.2:c.493-54del | NP_001012745.1:n.493-54del |