HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1414491_1414492insGGGTGGGGGGCCGGGAGGGGCAGGGCGGGGAAGGCACTGGGTGGGGGGCCTGGAGGGGCAGGGCGGGGAAGGCACTGGGTGGGGGGCCCCGGGAGGGG , CM000667.2:g.1414491_1414492insGGGTGGGGGGCCGGGAGGGGCAGGGCGGGGAAGGCACTGGGTGGGGGGCCTGGAGGGGCAGGGCGGGGAAGGCACTGGGTGGGGGGCCCCGGGAGGGG | GRCh38 |
NC_000005.9:g.1414606_1414607insGGGTGGGGGGCCGGGAGGGGCAGGGCGGGGAAGGCACTGGGTGGGGGGCCTGGAGGGGCAGGGCGGGGAAGGCACTGGGTGGGGGGCCCCGGGAGGGG , CM000667.1:g.1414606_1414607insGGGTGGGGGGCCGGGAGGGGCAGGGCGGGGAAGGCACTGGGTGGGGGGCCTGGAGGGGCAGGGCGGGGAAGGCACTGGGTGGGGGGCCCCGGGAGGGG | GRCh37 |
NC_000005.8:g.1467606_1467607insGGGTGGGGGGCCGGGAGGGGCAGGGCGGGGAAGGCACTGGGTGGGGGGCCTGGAGGGGCAGGGCGGGGAAGGCACTGGGTGGGGGGCCCCGGGAGGGG | NCBI36 |
NG_015885.1:g.35937_35938insCCCCTCCCGGGGCCCCCCACCCAGTGCCTTCCCCGCCCTGCCCCTCCAGGCCCCCCACCCAGTGCCTTCCCCGCCCTGCCCCTCCCGGCCCCCCACCC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270349.12:c.1156+199_1156+200insCCCCTCCCGGGGCCCCCCACCCAGTGCCTTCCCCGCCCTGCCCCTCCAGGCCCCCCACCCAGTGCCTTCCCCGCCCTGCCCCTCCCGGCCCCCCACCC MANE Select | ENSP00000270349.9:n.1156+199_1156+200insCCCCTCCCGGGGCCCCCCACC... | |
ENST00000270349.11:c.1156+199_1156+200insCCCCTCCCGGGGCCCCCCACCCAGTGCCTTCCCCGCCCTGCCCCTCCAGGCCCCCCACCCAGTGCCTTCCCCGCCCTGCCCCTCCCGGCCCCCCACCC | ENSP00000270349.9:n.1156+199_1156+200insCCCCTCCCGGGGCCCCCCACC... | |
NM_001044.4:c.1156+199_1156+200insCCCCTCCCGGGGCCCCCCACCCAGTGCCTTCCCCGCCCTGCCCCTCCAGGCCCCCCACCCAGTGCCTTCCCCGCCCTGCCCCTCCCGGCCCCCCACCC | NP_001035.1:n.1156+199_1156+200insCCCCTCCCGGGGCCCCCCACCCAGTGC... | |
NM_001044.5:c.1156+199_1156+200insCCCCTCCCGGGGCCCCCCACCCAGTGCCTTCCCCGCCCTGCCCCTCCAGGCCCCCCACCCAGTGCCTTCCCCGCCCTGCCCCTCCCGGCCCCCCACCC MANE Select | NP_001035.1:n.1156+199_1156+200insCCCCTCCCGGGGCCCCCCACCCAGTGC... |