Linked Data
gnomAD v4:
10-94942104-AGCTTG-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94942107_94942111del , CM000672.2:g.94942107_94942111del | GRCh38 |
| NC_000010.10:g.96701864_96701868del , CM000672.1:g.96701864_96701868del | GRCh37 |
| NC_000010.9:g.96691854_96691858del | NCBI36 |
| NG_008385.1:g.8450_8454del | |
| NG_008385.2:g.8950_8954del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000260682.8:c.332-85_332-81del MANE Select | ENSP00000260682.6:n.332-85_332-81del | |
| ENST00000643112.1:c.332-85_332-81del | ENSP00000496202.1:n.332-85_332-81del | |
| ENST00000645207.1:n.485-85_485-81del | ||
| ENST00000260682.6:c.332-85_332-81del | ENSP00000260682.6:n.332-85_332-81del | |
| ENST00000461906.1:n.357-85_357-81del | ||
| ENST00000473496.1:n.103-85_103-81del | ||
| NM_000771.3:c.332-85_332-81del | NP_000762.2:n.332-85_332-81del | |
| NM_000771.4:c.332-85_332-81del MANE Select | NP_000762.2:n.332-85_332-81del |