HGVS | Genome Assembly |
---|---|
NC_000017.11:g.5022632_5022658del , CM000679.2:g.5022632_5022658del | GRCh38 |
NC_000017.10:g.4925927_4925953del , CM000679.1:g.4925927_4925953del | GRCh37 |
NC_000017.9:g.4866651_4866677del | NCBI36 |
NG_034137.1:g.29685_29711del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320785.10:c.2551_2577del MANE Select | ENSP00000320821.5:p.Asn851_Gln859del | |
ENST00000320785.9:c.2551_2577del | ENSP00000320821.5:p.Asn851_Gln859del | |
NM_006612.5:c.2551_2577del | NP_006603.2:p.Asn851_Gln859del | |
XM_005256424.1:c.2551_2577del | XP_005256481.1:p.Asn851_Gln859del | |
XM_005256424.2:c.2551_2577del | XP_005256481.1:p.Asn851_Gln859del | |
NM_006612.6:c.2551_2577del MANE Select | NP_006603.2:p.Asn851_Gln859del |