HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42682546_42682547insTC , CM000679.2:g.42682546_42682547insTC | GRCh38 |
NC_000017.10:g.40834564_40834565insTC , CM000679.1:g.40834564_40834565insTC | GRCh37 |
NC_000017.9:g.38088090_38088091insTC | NCBI36 |
NG_042091.1:g.4933_4934insTC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264638.9:c.-284_-283insTC (CNTNAP1) MANE Select | ENSP00000264638.3:n.-284_-283insTC | |
ENST00000591568.1:c.-643+1270_-643+1271insAG (CCR10) | ENSP00000467331.1:n.-643+1270_-643+1271insAG | |
ENST00000591765.1:c.-868_-867insAG (CCR10) | ENSP00000468135.1:n.-868_-867insAG | |
XM_017025238.1:c.-284_-283insTC (CNTNAP1) | XP_016880727.1:n.-284_-283insTC | |
XM_024451011.1:c.-284_-283insTC (CNTNAP1) | XP_024306779.1:n.-284_-283insTC | |
NM_003632.3:c.-284_-283insTC (CNTNAP1) MANE Select | NP_003623.1:n.-284_-283insTC |