HGVS | Genome Assembly |
---|---|
NC_000003.12:g.190408187del , CM000665.2:g.190408187del | GRCh38 |
NC_000003.11:g.190125976del , CM000665.1:g.190125976del | GRCh37 |
NC_000003.10:g.191608670del | NCBI36 |
NG_008149.1:g.25136del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264734.3:c.383-127del MANE Select | ENSP00000264734.3:n.383-127del | |
ENST00000456423.2:c.115-1716del | ENSP00000414136.2:n.115-1716del | |
ENST00000264734.2:c.593-127del | ENSP00000264734.2:n.593-127del | |
ENST00000456423.1:c.325-1716del | ENSP00000414136.1:n.325-1716del | |
NM_006580.3:c.593-127del | NP_006571.1:n.593-127del | |
NM_001378492.1:c.383-127del | NP_001365421.1:n.383-127del | |
NM_001378493.1:c.383-127del | NP_001365422.1:n.383-127del | |
NM_006580.4:c.383-127del MANE Select | NP_006571.2:n.383-127del |