HGVS | Genome Assembly |
---|---|
NC_000004.12:g.68670246dup , CM000666.2:g.68670246dup | GRCh38 |
NC_000004.11:g.69535964dup , CM000666.1:g.69535964dup | GRCh37 |
NC_000004.10:g.69218559dup | NCBI36 |
NG_052676.1:g.5532dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000338206.6:c.374dup MANE Select | ENSP00000341045.5:p.Asn125LysfsTer5 | |
ENST00000338206.5:c.374dup | ENSP00000341045.5:p.Asn125LysfsTer5 | |
ENST00000616841.4:c.374dup | ENSP00000482004.1:p.Asn125LysfsTer5 | |
NM_001076.3:c.374dup | NP_001067.2:p.Asn125LysfsTer5 | |
NM_001076.4:c.374dup MANE Select | NP_001067.2:p.Asn125LysfsTer5 |