HGVS | Genome Assembly |
---|---|
NC_000012.12:g.69353493_69353494insTTTTTTTTTTTTT , CM000674.2:g.69353493_69353494insTTTTTTTTTTTTT | GRCh38 |
NC_000012.11:g.69747273_69747274insTTTTTTTTTTTTT , CM000674.1:g.69747273_69747274insTTTTTTTTTTTTT | GRCh37 |
NC_000012.10:g.68033540_68033541insTTTTTTTTTTTTT | NCBI36 |
NG_008195.1:g.10140_10141insTTTTTTTTTTTTT , LRG_768:g.10140_10141insTTTTTTTTTTTTT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261267.7:c.*274_*275insTTTTTTTTTTTTT MANE Select | ENSP00000261267.2:n.*274_*275insTTTTTTTTTTTTT | |
ENST00000261267.6:c.*274_*275insTTTTTTTTTTTTT | ENSP00000261267.2:n.*274_*275insTTTTTTTTTTTTT | |
ENST00000549690.1:c.*228_*229insTTTTTTTTTTTTT | ENSP00000449898.1:n.*228_*229insTTTTTTTTTTTTT | |
NM_000239.2:c.*274_*275insTTTTTTTTTTTTT , LRG_768t1:c.*274_*275insTTTTTTTTTTTTT | NP_000230.1:n.*274_*275insTTTTTTTTTTTTT | |
NM_000239.3:c.*274_*275insTTTTTTTTTTTTT MANE Select | NP_000230.1:n.*274_*275insTTTTTTTTTTTTT |