HGVS | Genome Assembly |
---|---|
NC_000004.12:g.68646741_68646742insTTTTTTTTTTTTTTT , CM000666.2:g.68646741_68646742insTTTTTTTTTTTTTTT | GRCh38 |
NC_000004.11:g.69512459_69512460insTTTTTTTTTTTTTTT , CM000666.1:g.69512459_69512460insTTTTTTTTTTTTTTT | GRCh37 |
NC_000004.10:g.69195054_69195055insTTTTTTTTTTTTTTT | NCBI36 |
NG_052676.1:g.29047_29048insAAAAAAAAAAAAAAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000338206.6:c.*374_*375insAAAAAAAAAAAAAAA MANE Select | ENSP00000341045.5:n.*374_*375insAAAAAAAAAAAAAAA | |
ENST00000338206.5:c.*374_*375insAAAAAAAAAAAAAAA | ENSP00000341045.5:n.*374_*375insAAAAAAAAAAAAAAA | |
ENST00000616841.4:c.1732+235_1732+236insAAAAAAAAAAAAAAA | ENSP00000482004.1:n.1732+235_1732+236insAAAAAAAAAAAAAAA | |
NM_001076.3:c.*374_*375insAAAAAAAAAAAAAAA | NP_001067.2:n.*374_*375insAAAAAAAAAAAAAAA | |
NM_001076.4:c.*374_*375insAAAAAAAAAAAAAAA MANE Select | NP_001067.2:n.*374_*375insAAAAAAAAAAAAAAA |