Linked Data
gnomAD v4:
17-34255897-T-TCC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.34255900_34255901dup , CM000679.2:g.34255900_34255901dup | GRCh38 |
| NC_000017.10:g.32582919_32582920dup , CM000679.1:g.32582919_32582920dup | GRCh37 |
| NC_000017.9:g.29607032_29607033dup | NCBI36 |
| NG_012123.1:g.5624_5625dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000580907.6:c.77-322_77-321dup | ENSP00000462156.1:n.77-322_77-321dup | |
| ENST00000624362.2:n.616_617dup | ||
| ENST00000225831.4:c.77-322_77-321dup MANE Select | ENSP00000225831.4:n.77-322_77-321dup | |
| ENST00000580907.5:c.77-322_77-321dup | ENSP00000462156.1:n.77-322_77-321dup | |
| ENST00000624362.1:n.683_684dup | ||
| NM_002982.3:c.77-322_77-321dup | NP_002973.1:n.77-322_77-321dup | |
| NM_002982.4:c.77-322_77-321dup MANE Select | NP_002973.1:n.77-322_77-321dup |