HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73322882_73322908del , CM000677.2:g.73322882_73322908del | GRCh38 |
NC_000015.9:g.73615223_73615249del , CM000677.1:g.73615223_73615249del | GRCh37 |
NC_000015.8:g.71402276_71402302del | NCBI36 |
NG_009063.1:g.51363_51389del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.3191_3217del MANE Select | ENSP00000261917.3:p.Gln1064_Pro1072del | |
ENST00000261917.3:c.3191_3217del | ENSP00000261917.3:p.Gln1064_Pro1072del | |
NM_005477.2:c.3191_3217del | NP_005468.1:p.Gln1064_Pro1072del | |
XM_011521148.1:c.1973_1999del | XP_011519450.1:p.Gln658_Pro666del | |
XM_011521148.2:c.1973_1999del | XP_011519450.1:p.Gln658_Pro666del | |
NM_005477.3:c.3191_3217del MANE Select | NP_005468.1:p.Gln1064_Pro1072del |