Linked Data
dbSNP Id:
rs1656136864
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.109264573_109264574insATCCT , CM000663.2:g.109264573_109264574insATCCT | GRCh38 |
| NC_000001.10:g.109807195_109807196insATCCT , CM000663.1:g.109807195_109807196insATCCT | GRCh37 |
| NC_000001.9:g.109608718_109608719insATCCT | NCBI36 |
| NG_052669.1:g.19869_19870insATCCT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271332.4:c.5409_5410insATCCT MANE Select | ENSP00000271332.3:p.Ala1804IlefsTer? | |
| ENST00000271332.3:c.5409_5410insATCCT | ENSP00000271332.3:p.Ala1804IlefsTer? | |
| NM_001408.2:c.5409_5410insATCCT | NP_001399.1:p.Ala1804IlefsTer? | |
| XM_005270580.3:c.5409_5410insATCCT | XP_005270637.1:p.Ala1804IlefsTer? | |
| NM_001408.3:c.5409_5410insATCCT MANE Select | NP_001399.1:p.Ala1804IlefsTer? |