HGVS | Genome Assembly |
---|---|
NC_000017.11:g.74917348dup , CM000679.2:g.74917348dup | GRCh38 |
NC_000017.10:g.72913442dup , CM000679.1:g.72913442dup | GRCh37 |
NC_000017.9:g.70425037dup | NCBI36 |
NG_007882.1:g.10912dup | |
NG_007882.2:g.10918dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000614341.5:c.*727dup MANE Select | ENSP00000480279.1:n.*727dup | |
ENST00000614341.4:c.*727dup | ENSP00000480279.1:n.*727dup | |
NM_001282489.2:c.*727dup | NP_001269418.1:n.*727dup | |
NM_173477.4:c.*727dup | NP_775748.2:n.*727dup | |
XM_011524296.1:c.*727dup | XP_011522598.1:n.*727dup | |
XM_011524296.2:c.*727dup | XP_011522598.1:n.*727dup | |
NM_173477.5:c.*727dup MANE Select | NP_775748.2:n.*727dup | |
NM_001282489.3:c.*727dup | NP_001269418.1:n.*727dup |