HGVS | Genome Assembly |
---|---|
NC_000007.14:g.107709950dup , CM000669.2:g.107709950dup | GRCh38 |
NC_000007.13:g.107350395dup , CM000669.1:g.107350395dup | GRCh37 |
NC_000007.12:g.107137631dup | NCBI36 |
NG_008489.1:g.54316dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000644269.2:c.2090-104dup MANE Select | ENSP00000494017.1:n.2090-104dup | |
ENST00000644846.1:c.746-104dup | ||
ENST00000265715.7:c.2090-104dup | ENSP00000265715.3:n.2090-104dup | |
ENST00000492030.2:n.377-205dup | ||
NM_000441.1:c.2090-104dup | NP_000432.1:n.2090-104dup | |
XM_005250425.1:c.2090-104dup | XP_005250482.1:n.2090-104dup | |
XM_005250425.2:c.2090-104dup | XP_005250482.1:n.2090-104dup | |
XM_017012318.1:c.2012-104dup | XP_016867807.1:n.2012-104dup | |
NM_000441.2:c.2090-104dup MANE Select | NP_000432.1:n.2090-104dup |