HGVS | Genome Assembly |
---|---|
NC_000001.11:g.215675614_215675615insAGA , CM000663.2:g.215675614_215675615insAGA | GRCh38 |
NC_000001.10:g.215848956_215848957insAGA , CM000663.1:g.215848956_215848957insAGA | GRCh37 |
NC_000001.9:g.213915579_213915580insAGA | NCBI36 |
NG_009497.1:g.752782_752783insTCT | |
NG_009497.2:g.752834_752835insTCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.12296_12297insTCT MANE Select | ENSP00000305941.3:p.Thr4099_Tyr4100insLeu | |
ENST00000674083.1:c.12296_12297insTCT | ENSP00000501296.1:p.Thr4099_Tyr4100insLeu | |
ENST00000307340.7:c.12296_12297insTCT | ENSP00000305941.3:p.Thr4099_Tyr4100insLeu | |
NM_206933.2:c.12296_12297insTCT | NP_996816.2:p.Thr4099_Tyr4100insLeu | |
NM_206933.3:c.12296_12297insTCT | NP_996816.2:p.Thr4099_Tyr4100insLeu | |
NM_206933.4:c.12296_12297insTCT MANE Select | NP_996816.3:p.Thr4099_Tyr4100insLeu |