HGVS | Genome Assembly |
---|---|
NC_000001.11:g.169555306dup , CM000663.2:g.169555306dup | GRCh38 |
NC_000001.10:g.169524544dup , CM000663.1:g.169524544dup | GRCh37 |
NC_000001.9:g.167791168dup | NCBI36 |
NG_011806.1:g.36229dup , LRG_553:g.36229dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367797.9:c.997dup MANE Select | ENSP00000356771.3:p.Thr333AsnfsTer5 | |
ENST00000367796.3:c.997dup | ENSP00000356770.3:p.Thr333AsnfsTer5 | |
ENST00000367797.7:c.997dup | ENSP00000356771.3:p.Thr333AsnfsTer5 | |
NM_000130.4:c.997dup , LRG_553t1:c.997dup | NP_000121.2:p.Thr333AsnfsTer5 | |
XM_017000660.2:c.586dup | XP_016856149.1:p.Thr196AsnfsTer5 | |
NM_000130.5:c.997dup MANE Select | NP_000121.2:p.Thr333AsnfsTer5 |