HGVS | Genome Assembly |
---|---|
NC_000017.11:g.39665601_39665608del , CM000679.2:g.39665601_39665608del | GRCh38 |
NC_000017.10:g.37821854_37821861del , CM000679.1:g.37821854_37821861del | GRCh37 |
NC_000017.9:g.35075380_35075387del | NCBI36 |
NG_008892.1:g.5256_5263del , LRG_210:g.5256_5263del | |
NG_042278.1:g.2621_2628del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000309889.3:c.111-115_111-108del MANE Select | ENSP00000312624.2:n.111-115_111-108del | |
ENST00000309889.2:c.111-115_111-108del | ENSP00000312624.2:n.111-115_111-108del | |
ENST00000578283.1:c.111-115_111-108del | ENSP00000462787.1:n.111-115_111-108del | |
NM_003673.3:c.111-115_111-108del , LRG_210t1:c.111-115_111-108del | NP_003664.1:n.111-115_111-108del | |
NM_003673.4:c.111-115_111-108del MANE Select | NP_003664.1:n.111-115_111-108del |