Canonical Allele Identifier: CA2230785012
Gene: COG4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.70481417G= , CM000678.2:g.70481417G= GRCh38
NC_000016.9:g.70515320G= , CM000678.1:g.70515320G= GRCh37
NC_000016.8:g.69072821G= NCBI36
NG_027529.1:g.47138C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000534772.2:c.*2253C= ENSP00000461912.2:n.*2253C=
ENST00000703106.1:c.2222C= ENSP00000515173.1:n.2222C=
ENST00000703107.1:c.*2106C= ENSP00000515174.1:n.*2106C=
ENST00000703108.1:c.*625C= ENSP00000515175.1:n.*625C=
ENST00000703109.1:c.2210C= ENSP00000515176.1:p.Thr737=
ENST00000703110.1:c.*1679C= ENSP00000515177.1:n.*1679C=
ENST00000703111.1:n.2460C=
ENST00000703112.1:n.3121C=
ENST00000703113.1:c.*1590C= ENSP00000515178.1:n.*1590C=
ENST00000703114.1:c.*826C= ENSP00000515179.1:n.*826C=
ENST00000703115.1:c.1290C= ENSP00000515180.1:n.1290C=
ENST00000323786.10:c.2177C= MANE Select ENSP00000315775.5:p.Thr726=
ENST00000564415.6:c.*1957C= ENSP00000456653.2:n.*1957C=
ENST00000674443.1:c.2102C= ENSP00000501405.1:p.Thr701=
ENST00000323786.9:c.2177C= ENSP00000315775.5:p.Thr726=
ENST00000393612.8:c.2114C= ENSP00000377236.5:p.Thr705=
ENST00000482252.5:c.2324C= ENSP00000432802.1:n.2324C=
ENST00000526700.5:n.1353C=
ENST00000530314.5:n.2856C=
ENST00000564415.5:c.*1957C= ENSP00000456653.1:n.*1957C=
ENST00000565715.1:c.239C= ENSP00000455693.1:p.Thr80=
NM_001195139.1:c.2114C= NP_001182068.1:p.Thr705=
NM_015386.2:c.2177C= NP_056201.2:p.Thr726=
XM_011522981.1:c.1751C= XP_011521283.1:p.Thr584=
XM_011522981.3:c.1751C= XP_011521283.1:p.Thr584=
XM_024450224.1:c.1196C= XP_024305992.1:p.Thr399=
XR_933266.2:n.2123C=
NM_015386.3:c.2177C= MANE Select NP_056201.2:p.Thr726=
NM_001195139.2:c.2102C= NP_001182068.2:p.Thr701=
NM_001365426.1:c.1751C= NP_001352355.1:p.Thr584=
NR_158212.1:n.2136C=