HGVS | Genome Assembly |
---|---|
NC_000005.10:g.37249498_37249499insAGAT , CM000667.2:g.37249498_37249499insAGAT | GRCh38 |
NC_000005.9:g.37249600_37249601insAGAT , CM000667.1:g.37249600_37249601insAGAT | GRCh37 |
NC_000005.8:g.37285357_37285358insAGAT | NCBI36 |
NG_032772.1:g.4930_4931insATCT | |
NG_032772.2:g.4930_4931insATCT |
HGVS | Amino-acid Change | |
---|---|---|
XR_925921.1:n.171+277_171+278insAGAT (CPLANE1-AS1) | ||
NR_134263.1:n.176+277_176+278insAGAT (CPLANE1-AS1) | ||
XM_005248345.4:c.-302_-301insATCT (CPLANE1) | XP_005248402.1:n.-302_-301insATCT | |
XM_005248346.4:c.-302_-301insATCT (CPLANE1) | XP_005248403.1:n.-302_-301insATCT | |
XM_005248347.4:c.-302_-301insATCT (CPLANE1) | XP_005248404.1:n.-302_-301insATCT | |
XM_005248349.4:c.-302_-301insATCT (CPLANE1) | XP_005248406.1:n.-302_-301insATCT | |
XM_005248350.4:c.-302_-301insATCT (CPLANE1) | XP_005248407.1:n.-302_-301insATCT |