HGVS | Genome Assembly |
---|---|
NC_000006.12:g.24290857_24290858insTTCTG , CM000668.2:g.24290857_24290858insTTCTG | GRCh38 |
NC_000006.11:g.24291085_24291086insTTCTG , CM000668.1:g.24291085_24291086insTTCTG | GRCh37 |
NC_000006.10:g.24399064_24399065insTTCTG | NCBI36 |
NG_012829.1:g.72195_72196insCAGAA | |
NG_012829.2:g.97435_97436insCAGAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378454.8:c.704+74_704+75insCAGAA MANE Select | ENSP00000367715.3:n.704+74_704+75insCAGAA | |
ENST00000378454.7:c.704+74_704+75insCAGAA | ENSP00000367715.3:n.704+74_704+75insCAGAA | |
NM_001195610.1:c.704+74_704+75insCAGAA | NP_001182539.1:n.704+74_704+75insCAGAA | |
NM_016356.4:c.704+74_704+75insCAGAA | NP_057440.2:n.704+74_704+75insCAGAA | |
NM_016356.5:c.704+74_704+75insCAGAA MANE Select | NP_057440.2:n.704+74_704+75insCAGAA | |
NM_001195610.2:c.704+74_704+75insCAGAA | NP_001182539.1:n.704+74_704+75insCAGAA |