HGVS | Genome Assembly |
---|---|
NC_000021.9:g.44456819_44456829delinsCCCGAGGACAT , CM000683.2:g.44456819_44456829delinsCCCGAGGACAT | GRCh38 |
NC_000021.8:g.45876702_45876712delinsCCCGAGGACAT , CM000683.1:g.45876702_45876712delinsCCCGAGGACAT | GRCh37 |
NC_000021.7:g.44701130_44701140delinsCCCGAGGACAT | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291592.6:c.175_185delinsCCCGAGGACAT MANE Select | ENSP00000291592.4:p.Pro59= | |
ENST00000291592.5:c.175_185delinsCCCGAGGACAT | ENSP00000291592.4:p.Pro59= | |
NM_030891.4:c.175_185delinsCCCGAGGACAT | NP_112153.1:p.Pro59= | |
NM_030891.5:c.175_185delinsCCCGAGGACAT | NP_112153.1:p.Pro59= | |
NM_030891.6:c.175_185delinsCCCGAGGACAT MANE Select | NP_112153.1:p.Pro59= |