HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42682564_42682565insCT , CM000679.2:g.42682564_42682565insCT | GRCh38 |
NC_000017.10:g.40834582_40834583insCT , CM000679.1:g.40834582_40834583insCT | GRCh37 |
NC_000017.9:g.38088108_38088109insCT | NCBI36 |
NG_042091.1:g.4951_4952insCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264638.9:c.-266_-265insCT (CNTNAP1) MANE Select | ENSP00000264638.3:n.-266_-265insCT | |
ENST00000591568.1:c.-643+1251_-643+1252insAG (CCR10) | ENSP00000467331.1:n.-643+1251_-643+1252insAG | |
ENST00000591765.1:c.-887_-886insAG (CCR10) | ENSP00000468135.1:n.-887_-886insAG | |
XM_017025238.1:c.-266_-265insCT (CNTNAP1) | XP_016880727.1:n.-266_-265insCT | |
XM_024451011.1:c.-266_-265insCT (CNTNAP1) | XP_024306779.1:n.-266_-265insCT | |
NM_003632.3:c.-266_-265insCT (CNTNAP1) MANE Select | NP_003623.1:n.-266_-265insCT |