HGVS | Genome Assembly |
---|---|
NC_000017.11:g.5002445dup , CM000679.2:g.5002445dup | GRCh38 |
NC_000017.10:g.4905740dup , CM000679.1:g.4905740dup | GRCh37 |
NC_000017.9:g.4846464dup | NCBI36 |
NG_034137.1:g.9498dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320785.10:c.430-19dup (KIF1C) MANE Select | ENSP00000320821.5:n.430-19dup | |
ENST00000320785.9:c.430-19dup (KIF1C) | ENSP00000320821.5:n.430-19dup | |
NM_006612.5:c.430-19dup (KIF1C) | NP_006603.2:n.430-19dup | |
XM_005256424.1:c.430-19dup (KIF1C) | XP_005256481.1:n.430-19dup | |
XM_005256424.2:c.430-19dup (KIF1C) | XP_005256481.1:n.430-19dup | |
XM_024450745.1:c.-39+3637dup (INCA1) | XP_024306513.1:n.-39+3637dup | |
NM_006612.6:c.430-19dup (KIF1C) MANE Select | NP_006603.2:n.430-19dup |