HGVS | Genome Assembly |
---|---|
NC_000021.9:g.31663985_31663990del , CM000683.2:g.31663985_31663990del | GRCh38 |
NC_000021.8:g.33036298_33036303del , CM000683.1:g.33036298_33036303del | GRCh37 |
NC_000021.7:g.31958169_31958174del | NCBI36 |
NG_008689.1:g.9364_9369del , LRG_652:g.9364_9369del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270142.11:c.169+99_169+104del MANE Select | ENSP00000270142.7:n.169+99_169+104del | |
ENST00000270142.10:c.169+99_169+104del | ENSP00000270142.6:n.169+99_169+104del | |
ENST00000389995.4:c.112+99_112+104del | ENSP00000374645.4:n.112+99_112+104del | |
ENST00000470944.1:n.1097+99_1097+104del | ||
ENST00000476106.5:n.432+99_432+104del | ||
NM_000454.4:c.169+99_169+104del , LRG_652t1:c.169+99_169+104del | NP_000445.1:n.169+99_169+104del | |
NM_000454.5:c.169+99_169+104del MANE Select | NP_000445.1:n.169+99_169+104del |