HGVS | Genome Assembly |
---|---|
NC_000001.11:g.1013880_1013904dup , CM000663.2:g.1013880_1013904dup | GRCh38 |
NC_000001.10:g.949260_949284dup , CM000663.1:g.949260_949284dup | GRCh37 |
NC_000001.9:g.939123_939147dup | NCBI36 |
NG_033033.1:g.5414_5438dup | |
NG_033033.2:g.17743_17767dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000624697.4:c.-21-104_-21-80dup | ENSP00000485643.1:n.-21-104_-21-80dup | |
ENST00000649529.1:c.4-104_4-80dup MANE Select | ENSP00000496832.1:n.4-104_4-80dup | |
ENST00000379389.4:c.4-104_4-80dup | ENSP00000368699.4:n.4-104_4-80dup | |
ENST00000624652.1:c.-21-104_-21-80dup | ENSP00000485313.1:n.-21-104_-21-80dup | |
ENST00000624697.3:c.-21-104_-21-80dup | ENSP00000485643.1:n.-21-104_-21-80dup | |
NM_005101.3:c.4-104_4-80dup | NP_005092.1:n.4-104_4-80dup | |
NM_005101.4:c.4-104_4-80dup MANE Select | NP_005092.1:n.4-104_4-80dup |