HGVS | Genome Assembly |
---|---|
NC_000021.9:g.43416598_43416602del , CM000683.2:g.43416598_43416602del | GRCh38 |
NG_052009.1:g.15535_15539del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270162.8:c.*144_*148del MANE Select | ENSP00000270162.6:n.*144_*148del | |
ENST00000270162.6:c.*144_*148del | ENSP00000270162.6:n.*144_*148del | |
NM_173354.3:c.*144_*148del | NP_775490.2:n.*144_*148del | |
XM_011529474.1:c.*144_*148del | XP_011527776.1:n.*144_*148del | |
NM_173354.4:c.*144_*148del | NP_775490.2:n.*144_*148del | |
XM_011529474.2:c.*144_*148del | XP_011527776.1:n.*144_*148del | |
NM_173354.5:c.*144_*148del MANE Select | NP_775490.2:n.*144_*148del |