HGVS | Genome Assembly |
---|---|
NC_000019.10:g.40845143_40845150dup , CM000681.2:g.40845143_40845150dup | GRCh38 |
NC_000019.9:g.41351048_41351055dup , CM000681.1:g.41351048_41351055dup | GRCh37 |
NC_000019.8:g.46042888_46042895dup | NCBI36 |
NG_008377.1:g.10304_10311dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301141.10:c.1161+150_1161+157dup MANE Select | ENSP00000301141.4:n.1161+150_1161+157dup | |
ENST00000301141.9:c.1161+150_1161+157dup | ENSP00000301141.4:n.1161+150_1161+157dup | |
ENST00000596719.5:n.1162_1169dup | ||
ENST00000601627.1:c.119+43728_119+43735dup | ||
ENST00000610301.1:c.1161+150_1161+157dup | ENSP00000477899.1:n.1161+150_1161+157dup | |
NM_000762.5:c.1161+150_1161+157dup | NP_000753.3:n.1161+150_1161+157dup | |
NM_000762.6:c.1161+150_1161+157dup MANE Select | NP_000753.3:n.1161+150_1161+157dup |