HGVS | Genome Assembly |
---|---|
NC_000007.14:g.97006082_97006105del , CM000669.2:g.97006082_97006105del | GRCh38 |
NC_000007.13:g.96635394_96635417del , CM000669.1:g.96635394_96635417del | GRCh37 |
NC_000007.12:g.96473330_96473353del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000518156.3:c.105_128del (DLX6) MANE Select | ENSP00000428480.2:p.Gln36_Gln43del | |
ENST00000518156.2:c.105_128del (DLX6) | ENSP00000428480.2:p.Gln36_Gln43del | |
NM_005222.3:c.105_128del (DLX6) | NP_005213.3:p.Gln36_Gln43del | |
NR_015448.1:n.141+7849_141+7872del (DLX6-AS1) | ||
NM_005222.4:c.105_128del (DLX6) MANE Select | NP_005213.3:p.Gln36_Gln43del |