Canonical Allele Identifier: CA2230785001
Gene: COG4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.70481397G= , CM000678.2:g.70481397G= GRCh38
NC_000016.9:g.70515300G= , CM000678.1:g.70515300G= GRCh37
NC_000016.8:g.69072801G= NCBI36
NG_027529.1:g.47158C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000534772.2:c.*2273C= ENSP00000461912.2:n.*2273C=
ENST00000703106.1:c.2242C= ENSP00000515173.1:n.2242C=
ENST00000703107.1:c.*2126C= ENSP00000515174.1:n.*2126C=
ENST00000703108.1:c.*645C= ENSP00000515175.1:n.*645C=
ENST00000703109.1:c.2230C= ENSP00000515176.1:p.Arg744=
ENST00000703110.1:c.*1699C= ENSP00000515177.1:n.*1699C=
ENST00000703111.1:n.2480C=
ENST00000703112.1:n.3141C=
ENST00000703113.1:c.*1610C= ENSP00000515178.1:n.*1610C=
ENST00000703114.1:c.*846C= ENSP00000515179.1:n.*846C=
ENST00000703115.1:c.1310C= ENSP00000515180.1:n.1310C=
ENST00000323786.10:c.2197C= MANE Select ENSP00000315775.5:p.Arg733=
ENST00000564415.6:c.*1977C= ENSP00000456653.2:n.*1977C=
ENST00000674443.1:c.2122C= ENSP00000501405.1:p.Arg708=
ENST00000323786.9:c.2197C= ENSP00000315775.5:p.Arg733=
ENST00000393612.8:c.2134C= ENSP00000377236.5:p.Arg712=
ENST00000482252.5:c.2344C= ENSP00000432802.1:n.2344C=
ENST00000526700.5:n.1373C=
ENST00000530314.5:n.2876C=
ENST00000564415.5:c.*1977C= ENSP00000456653.1:n.*1977C=
ENST00000565715.1:c.259C= ENSP00000455693.1:p.Arg87=
NM_001195139.1:c.2134C= NP_001182068.1:p.Arg712=
NM_015386.2:c.2197C= NP_056201.2:p.Arg733=
XM_011522981.1:c.1771C= XP_011521283.1:p.Arg591=
XM_011522981.3:c.1771C= XP_011521283.1:p.Arg591=
XM_024450224.1:c.1216C= XP_024305992.1:p.Arg406=
XR_933266.2:n.2143C=
NM_015386.3:c.2197C= MANE Select NP_056201.2:p.Arg733=
NM_001195139.2:c.2122C= NP_001182068.2:p.Arg708=
NM_001365426.1:c.1771C= NP_001352355.1:p.Arg591=
NR_158212.1:n.2156C=