HGVS | Genome Assembly |
---|---|
NC_000008.11:g.118111427_118111428insACACAA , CM000670.2:g.118111427_118111428insACACAA | GRCh38 |
NC_000008.10:g.119123666_119123667insACACAA , CM000670.1:g.119123666_119123667insACACAA | GRCh37 |
NC_000008.9:g.119192847_119192848insACACAA | NCBI36 |
NG_007455.2:g.5392_5393insTTGTGT , LRG_493:g.5392_5393insTTGTGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378204.7:c.-382_-381insTTGTGT MANE Select | ENSP00000367446.3:n.-382_-381insTTGTGT | |
ENST00000378204.6:c.-382_-381insTTGTGT | ENSP00000367446.2:n.-382_-381insTTGTGT | |
NM_000127.2:c.-382_-381insTTGTGT , LRG_493t1:c.-382_-381insTTGTGT | NP_000118.2:n.-382_-381insTTGTGT | |
NM_000127.3:c.-382_-381insTTGTGT MANE Select | NP_000118.2:n.-382_-381insTTGTGT |