HGVS | Genome Assembly |
---|---|
NC_000007.14:g.21881233del , CM000669.2:g.21881233del | GRCh38 |
NC_000007.13:g.21920851del , CM000669.1:g.21920851del | GRCh37 |
NC_000007.12:g.21887376del | NCBI36 |
NG_012886.2:g.343019del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000409508.8:c.12387+340del MANE Select | ENSP00000475939.1:n.12387+340del | |
ENST00000328843.10:c.12408+340del | ENSP00000330671.7:n.12408+340del | |
ENST00000409508.7:c.12387+340del | ENSP00000475939.1:n.12387+340del | |
ENST00000620169.4:c.12408+340del | ENSP00000481693.1:n.12408+340del | |
NM_001277115.1:c.12387+340del | NP_001264044.1:n.12387+340del | |
NM_001277115.2:c.12387+340del MANE Select | NP_001264044.1:n.12387+340del |