Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42682605_42682663del , CM000679.2:g.42682605_42682663del | GRCh38 |
| NC_000017.10:g.40834623_40834681del , CM000679.1:g.40834623_40834681del | GRCh37 |
| NC_000017.9:g.38088149_38088207del | NCBI36 |
| NG_042091.1:g.4992_5050del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264638.9:c.-225_-167del (CNTNAP1) MANE Select | ENSP00000264638.3:n.-225_-167del | |
| ENST00000591568.1:c.-643+1160_-643+1218del (CCR10) | ENSP00000467331.1:n.-643+1160_-643+1218del | |
| ENST00000591765.1:c.-978_-920del (CCR10) | ENSP00000468135.1:n.-978_-920del | |
| XM_017025238.1:c.-225_-167del (CNTNAP1) | XP_016880727.1:n.-225_-167del | |
| XM_024451011.1:c.-225_-167del (CNTNAP1) | XP_024306779.1:n.-225_-167del | |
| NM_003632.3:c.-225_-167del (CNTNAP1) MANE Select | NP_003623.1:n.-225_-167del |