HGVS | Genome Assembly |
---|---|
NC_000003.12:g.119414342dup , CM000665.2:g.119414342dup | GRCh38 |
NC_000003.11:g.119133189dup , CM000665.1:g.119133189dup | GRCh37 |
NC_000003.10:g.120615879dup | NCBI36 |
NG_007665.2:g.124970dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264245.9:c.2413dup MANE Select | ENSP00000264245.4:p.Glu805GlyfsTer25 | |
ENST00000264245.8:c.2413dup | ENSP00000264245.4:p.Glu805GlyfsTer25 | |
NM_020754.3:c.2413dup | NP_065805.2:p.Glu805GlyfsTer25 | |
XM_005247671.3:c.2320dup | XP_005247728.1:p.Glu774GlyfsTer25 | |
XM_006713714.2:c.2353dup | XP_006713777.1:p.Glu785GlyfsTer25 | |
XM_006713714.3:c.2353dup | XP_006713777.1:p.Glu785GlyfsTer25 | |
XM_017006955.1:c.1921dup | XP_016862444.1:p.Glu641GlyfsTer25 | |
NM_020754.4:c.2413dup MANE Select | NP_065805.2:p.Glu805GlyfsTer25 |