HGVS | Genome Assembly |
---|---|
NC_000004.12:g.55110598_55110601del , CM000666.2:g.55110598_55110601del | GRCh38 |
NC_000004.11:g.55976765_55976768del , CM000666.1:g.55976765_55976768del | GRCh37 |
NC_000004.10:g.55671522_55671525del | NCBI36 |
NG_012004.1:g.19996_19999del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263923.5:c.1092-34_1092-31del MANE Select | ENSP00000263923.4:n.1092-34_1092-31del | |
ENST00000647068.1:n.1105-34_1105-31del | ||
ENST00000263923.4:c.1092-34_1092-31del | ENSP00000263923.4:n.1092-34_1092-31del | |
ENST00000512566.1:n.1092-34_1092-31del | ||
NM_002253.2:c.1092-34_1092-31del | NP_002244.1:n.1092-34_1092-31del | |
NM_002253.3:c.1092-34_1092-31del | NP_002244.1:n.1092-34_1092-31del | |
NM_002253.4:c.1092-34_1092-31del MANE Select | NP_002244.1:n.1092-34_1092-31del |