HGVS | Genome Assembly |
---|---|
NC_000023.11:g.25013692_25013697dup , CM000685.2:g.25013692_25013697dup | GRCh38 |
NC_000023.10:g.25031809_25031814dup , CM000685.1:g.25031809_25031814dup | GRCh37 |
NC_000023.9:g.24941730_24941735dup | NCBI36 |
NG_008281.1:g.7257_7262dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379044.5:c.303_308dup MANE Select | ENSP00000368332.4:p.Ala103_Ala104insAlaAla | |
ENST00000379044.4:c.303_308dup | ENSP00000368332.4:p.Ala103_Ala104insAlaAla | |
NM_139058.2:c.303_308dup | NP_620689.1:p.Ala103_Ala104insAlaAla | |
NM_139058.3:c.303_308dup MANE Select | NP_620689.1:p.Ala103_Ala104insAlaAla |