HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42682615_42682643del , CM000679.2:g.42682615_42682643del | GRCh38 |
NC_000017.10:g.40834633_40834661del , CM000679.1:g.40834633_40834661del | GRCh37 |
NC_000017.9:g.38088159_38088187del | NCBI36 |
NG_042091.1:g.5002_5030del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264638.9:c.-215_-187del (CNTNAP1) MANE Select | ENSP00000264638.3:n.-215_-187del | |
ENST00000591568.1:c.-643+1182_-643+1210del (CCR10) | ENSP00000467331.1:n.-643+1182_-643+1210del | |
ENST00000591765.1:c.-956_-928del (CCR10) | ENSP00000468135.1:n.-956_-928del | |
XM_017025238.1:c.-215_-187del (CNTNAP1) | XP_016880727.1:n.-215_-187del | |
XM_024451011.1:c.-215_-187del (CNTNAP1) | XP_024306779.1:n.-215_-187del | |
NM_003632.3:c.-215_-187del (CNTNAP1) MANE Select | NP_003623.1:n.-215_-187del |