Canonical Allele Identifier: CA2230762864
Gene: COG4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.70483866C= , CM000678.2:g.70483866C= GRCh38
NC_000016.9:g.70517769C= , CM000678.1:g.70517769C= GRCh37
NC_000016.8:g.69075270C= NCBI36
NG_027529.1:g.44689G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000534772.2:c.*1890G= ENSP00000461912.2:n.*1890G=
ENST00000703106.1:c.1859G= ENSP00000515173.1:n.1859G=
ENST00000703107.1:c.*1743G= ENSP00000515174.1:n.*1743G=
ENST00000703108.1:c.*262G= ENSP00000515175.1:n.*262G=
ENST00000703109.1:c.1847G= ENSP00000515176.1:p.Arg616=
ENST00000703110.1:c.*1316G= ENSP00000515177.1:n.*1316G=
ENST00000703111.1:n.1821G=
ENST00000703112.1:n.2587G=
ENST00000703113.1:c.*1227G= ENSP00000515178.1:n.*1227G=
ENST00000703114.1:c.*463G= ENSP00000515179.1:n.*463G=
ENST00000703115.1:c.927G= ENSP00000515180.1:n.927G=
ENST00000323786.10:c.1814G= MANE Select ENSP00000315775.5:p.Arg605=
ENST00000564415.6:c.*1594G= ENSP00000456653.2:n.*1594G=
ENST00000674443.1:c.1739G= ENSP00000501405.1:p.Arg580=
ENST00000323786.9:c.1814G= ENSP00000315775.5:p.Arg605=
ENST00000393612.8:c.1751G= ENSP00000377236.5:p.Arg584=
ENST00000482252.5:c.1961G= ENSP00000432802.1:n.1961G=
ENST00000526700.5:n.990G=
ENST00000530314.5:n.2493G=
ENST00000564315.1:n.274G=
ENST00000564415.5:c.*1594G= ENSP00000456653.1:n.*1594G=
NM_001195139.1:c.1751G= NP_001182068.1:p.Arg584=
NM_015386.2:c.1814G= NP_056201.2:p.Arg605=
XM_011522981.1:c.1388G= XP_011521283.1:p.Arg463=
XR_933266.1:n.1760G=
XR_933267.1:n.1760G=
XM_011522981.3:c.1388G= XP_011521283.1:p.Arg463=
XM_024450224.1:c.833G= XP_024305992.1:p.Arg278=
XR_001751889.1:n.1697G=
XR_933266.2:n.1760G=
NM_015386.3:c.1814G= MANE Select NP_056201.2:p.Arg605=
NM_001195139.2:c.1739G= NP_001182068.2:p.Arg580=
NM_001365426.1:c.1388G= NP_001352355.1:p.Arg463=
NR_158212.1:n.1773G=