HGVS | Genome Assembly |
---|---|
NC_000012.12:g.121627258_121627264dup , CM000674.2:g.121627258_121627264dup | GRCh38 |
NC_000012.11:g.122065164_122065170dup , CM000674.1:g.122065164_122065170dup | GRCh37 |
NC_000012.10:g.120549547_120549553dup | NCBI36 |
NG_007500.1:g.5684_5690dup , LRG_93:g.5684_5690dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698901.1:n.425+325_425+331dup | ||
ENST00000617316.2:c.303+208_303+214dup | ENSP00000482568.2:n.303+208_303+214dup | |
ENST00000646827.1:n.501+208_501+214dup | ||
ENST00000611718.1:c.238+84_238+90dup | ENSP00000477953.1:n.238+84_238+90dup | |
ENST00000616379.1:c.303+208_303+214dup | ENSP00000480616.1:n.303+208_303+214dup | |
ENST00000617316.1:c.114+208_114+214dup | ENSP00000482568.1:n.114+208_114+214dup | |
NM_032790.3:c.303+208_303+214dup , LRG_93t1:c.303+208_303+214dup | NP_116179.2:n.303+208_303+214dup |