HGVS | Genome Assembly |
---|---|
NC_000004.12:g.88008029_88008040del , CM000666.2:g.88008029_88008040del | GRCh38 |
NC_000004.11:g.88929181_88929192del , CM000666.1:g.88929181_88929192del | GRCh37 |
NC_000004.10:g.89148205_89148216del | NCBI36 |
NG_008604.1:g.5362_5373del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000237596.7:c.296_307del MANE Select | ENSP00000237596.2:p.Glu99_Glu102del | |
ENST00000237596.6:c.296_307del | ENSP00000237596.2:p.Glu99_Glu102del | |
NM_000297.3:c.296_307del | NP_000288.1:p.Glu99_Glu102del | |
XM_011532028.1:c.296_307del | XP_011530330.1:p.Glu99_Glu102del | |
XR_244632.2:n.391_402del | ||
NR_156488.1:n.383_394del | ||
XM_011532028.2:c.296_307del | XP_011530330.1:p.Glu99_Glu102del | |
NM_000297.4:c.296_307del MANE Select | NP_000288.1:p.Glu99_Glu102del | |
NR_156488.2:n.395_406del |