HGVS | Genome Assembly |
---|---|
NC_000004.12:g.67740670dup , CM000666.2:g.67740670dup | GRCh38 |
NC_000004.11:g.68606388dup , CM000666.1:g.68606388dup | GRCh37 |
NC_000004.10:g.68288983dup | NCBI36 |
NG_009293.1:g.20417dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000226413.5:c.797dup MANE Select | ENSP00000226413.5:p.Met268AsnfsTer26 | |
ENST00000226413.4:c.797dup | ENSP00000226413.4:p.Met268AsnfsTer26 | |
ENST00000420975.2:c.669dup | ENSP00000397561.2:p.Lys224Ter | |
NM_000406.2:c.797dup | NP_000397.1:p.Met268AsnfsTer26 | |
NM_001012763.1:c.669dup | NP_001012781.1:p.Lys224Ter | |
NM_000406.3:c.797dup MANE Select | NP_000397.1:p.Met268AsnfsTer26 | |
NM_001012763.2:c.669dup | NP_001012781.1:p.Lys224Ter |