HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52520333_52520334del , CM000674.2:g.52520333_52520334del | GRCh38 |
NC_000012.11:g.52914117_52914118del , CM000674.1:g.52914117_52914118del | GRCh37 |
NC_000012.10:g.51200384_51200385del | NCBI36 |
NG_008297.1:g.5126_5127del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252242.9:c.-38_-37del MANE Select | ENSP00000252242.4:n.-38_-37del | |
ENST00000252242.8:c.-38_-37del | ENSP00000252242.4:n.-38_-37del | |
ENST00000546577.1:c.-12-26_-12-25del | ENSP00000449651.1:n.-12-26_-12-25del | |
ENST00000549420.1:c.-38_-37del | ENSP00000447209.1:n.-38_-37del | |
ENST00000551275.1:c.-38_-37del | ENSP00000448041.1:n.-38_-37del | |
ENST00000552629.5:n.61_62del | ||
NM_000424.3:c.-38_-37del | NP_000415.2:n.-38_-37del | |
NM_000424.4:c.-38_-37del MANE Select | NP_000415.2:n.-38_-37del |