Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42682609_42682667del , CM000679.2:g.42682609_42682667del | GRCh38 |
| NC_000017.10:g.40834627_40834685del , CM000679.1:g.40834627_40834685del | GRCh37 |
| NC_000017.9:g.38088153_38088211del | NCBI36 |
| NG_042091.1:g.4996_5054del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264638.9:c.-221_-163del (CNTNAP1) MANE Select | ENSP00000264638.3:n.-221_-163del | |
| ENST00000591568.1:c.-643+1152_-643+1210del (CCR10) | ENSP00000467331.1:n.-643+1152_-643+1210del | |
| ENST00000591765.1:c.-986_-928del (CCR10) | ENSP00000468135.1:n.-986_-928del | |
| XM_017025238.1:c.-221_-163del (CNTNAP1) | XP_016880727.1:n.-221_-163del | |
| XM_024451011.1:c.-221_-163del (CNTNAP1) | XP_024306779.1:n.-221_-163del | |
| NM_003632.3:c.-221_-163del (CNTNAP1) MANE Select | NP_003623.1:n.-221_-163del |