HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52038115_52038128del , CM000666.2:g.52038115_52038128del | GRCh38 |
NC_000004.11:g.52904281_52904294del , CM000666.1:g.52904281_52904294del | GRCh37 |
NC_000004.10:g.52599038_52599051del | NCBI36 |
NG_008891.1:g.5192_5205del , LRG_204:g.5192_5205del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.10:c.33+99_33+112del MANE Select | ENSP00000370839.6:n.33+99_33+112del | |
ENST00000381431.9:c.33+99_33+112del | ENSP00000370839.5:n.33+99_33+112del | |
ENST00000506357.5:c.19+99_19+112del | ||
NM_000232.4:c.33+99_33+112del , LRG_204t1:c.33+99_33+112del | NP_000223.1:n.33+99_33+112del | |
XM_011534403.1:c.33+99_33+112del | XP_011532705.1:n.33+99_33+112del | |
NM_000232.5:c.33+99_33+112del MANE Select | NP_000223.1:n.33+99_33+112del |