HGVS | Genome Assembly |
---|---|
NC_000014.9:g.24255880_24255895dup , CM000676.2:g.24255880_24255895dup | GRCh38 |
NC_000014.8:g.24725086_24725101dup , CM000676.1:g.24725086_24725101dup | GRCh37 |
NC_000014.7:g.23794926_23794941dup | NCBI36 |
NG_007150.1:g.12279_12294dup | |
NG_007150.2:g.12279_12294dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000206765.11:c.1491+101_1491+116dup MANE Select | ENSP00000206765.6:n.1491+101_1491+116dup | |
ENST00000206765.10:c.1491+101_1491+116dup | ENSP00000206765.6:n.1491+101_1491+116dup | |
ENST00000544573.5:c.165+101_165+116dup | ENSP00000439446.1:n.165+101_165+116dup | |
ENST00000559136.1:c.564+101_564+116dup | ENSP00000453337.1:n.564+101_564+116dup | |
NM_000359.2:c.1491+101_1491+116dup | NP_000350.1:n.1491+101_1491+116dup | |
NM_000359.3:c.1491+101_1491+116dup MANE Select | NP_000350.1:n.1491+101_1491+116dup |