Canonical Allele Identifier: CA2230785030
Gene: COG4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.70481453G= , CM000678.2:g.70481453G= GRCh38
NC_000016.9:g.70515356G= , CM000678.1:g.70515356G= GRCh37
NC_000016.8:g.69072857G= NCBI36
NG_027529.1:g.47102C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000534772.2:c.*2217C= ENSP00000461912.2:n.*2217C=
ENST00000703106.1:c.2186C= ENSP00000515173.1:n.2186C=
ENST00000703107.1:c.*2070C= ENSP00000515174.1:n.*2070C=
ENST00000703108.1:c.*589C= ENSP00000515175.1:n.*589C=
ENST00000703109.1:c.2174C= ENSP00000515176.1:p.Ser725=
ENST00000703110.1:c.*1643C= ENSP00000515177.1:n.*1643C=
ENST00000703111.1:n.2424C=
ENST00000703112.1:n.3085C=
ENST00000703113.1:c.*1554C= ENSP00000515178.1:n.*1554C=
ENST00000703114.1:c.*790C= ENSP00000515179.1:n.*790C=
ENST00000703115.1:c.1254C= ENSP00000515180.1:n.1254C=
ENST00000323786.10:c.2141C= MANE Select ENSP00000315775.5:p.Ser714=
ENST00000564415.6:c.*1921C= ENSP00000456653.2:n.*1921C=
ENST00000674443.1:c.2066C= ENSP00000501405.1:p.Ser689=
ENST00000323786.9:c.2141C= ENSP00000315775.5:p.Ser714=
ENST00000393612.8:c.2078C= ENSP00000377236.5:p.Ser693=
ENST00000482252.5:c.2288C= ENSP00000432802.1:n.2288C=
ENST00000526700.5:n.1317C=
ENST00000530314.5:n.2820C=
ENST00000564415.5:c.*1921C= ENSP00000456653.1:n.*1921C=
ENST00000565715.1:c.203C= ENSP00000455693.1:p.Ser68=
NM_001195139.1:c.2078C= NP_001182068.1:p.Ser693=
NM_015386.2:c.2141C= NP_056201.2:p.Ser714=
XM_011522981.1:c.1715C= XP_011521283.1:p.Ser572=
XM_011522981.3:c.1715C= XP_011521283.1:p.Ser572=
XM_024450224.1:c.1160C= XP_024305992.1:p.Ser387=
XR_933266.2:n.2087C=
NM_015386.3:c.2141C= MANE Select NP_056201.2:p.Ser714=
NM_001195139.2:c.2066C= NP_001182068.2:p.Ser689=
NM_001365426.1:c.1715C= NP_001352355.1:p.Ser572=
NR_158212.1:n.2100C=