Canonical Allele Identifier: CA2230762783
Gene: COG4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.70483781G= , CM000678.2:g.70483781G= GRCh38
NC_000016.9:g.70517684G= , CM000678.1:g.70517684G= GRCh37
NC_000016.8:g.69075185G= NCBI36
NG_027529.1:g.44774C=

Transcript Alleles

HGVS Amino-acid change
ENST00000534772.2:c.*1903+72C= ENSP00000461912.2:n.*1903+72C=
ENST00000703106.1:c.1872+72C= ENSP00000515173.1:n.1872+72C=
ENST00000703107.1:c.*1756+72C= ENSP00000515174.1:n.*1756+72C=
ENST00000703108.1:c.*275+72C= ENSP00000515175.1:n.*275+72C=
ENST00000703109.1:c.1860+72C= ENSP00000515176.1:n.1860+72C=
ENST00000703110.1:c.*1329+72C= ENSP00000515177.1:n.*1329+72C=
ENST00000703111.1:n.1834+72C=
ENST00000703112.1:n.2600+72C=
ENST00000703113.1:c.*1240+72C= ENSP00000515178.1:n.*1240+72C=
ENST00000703114.1:c.*476+72C= ENSP00000515179.1:n.*476+72C=
ENST00000703115.1:c.940+72C= ENSP00000515180.1:n.940+72C=
ENST00000323786.10:c.1827+72C= MANE Select ENSP00000315775.5:n.1827+72C=
ENST00000564415.6:c.*1607+72C= ENSP00000456653.2:n.*1607+72C=
ENST00000674443.1:c.1752+72C= ENSP00000501405.1:n.1752+72C=
ENST00000323786.9:c.1827+72C= ENSP00000315775.5:n.1827+72C=
ENST00000393612.8:c.1764+72C= ENSP00000377236.5:n.1764+72C=
ENST00000482252.5:c.1974+72C= ENSP00000432802.1:n.1974+72C=
ENST00000526700.5:n.1003+72C=
ENST00000530314.5:n.2506+72C=
ENST00000564315.1:n.287+72C=
ENST00000564415.5:c.*1607+72C= ENSP00000456653.1:n.*1607+72C=
NM_001195139.1:c.1764+72C= NP_001182068.1:n.1764+72C=
NM_015386.2:c.1827+72C= NP_056201.2:n.1827+72C=
XM_011522981.1:c.1401+72C= XP_011521283.1:n.1401+72C=
XR_933266.1:n.1773+72C=
XR_933267.1:n.1773+72C=
XM_011522981.3:c.1401+72C= XP_011521283.1:n.1401+72C=
XM_024450224.1:c.846+72C= XP_024305992.1:n.846+72C=
XR_001751889.1:n.1710+72C=
XR_933266.2:n.1773+72C=
NM_015386.3:c.1827+72C= MANE Select NP_056201.2:n.1827+72C=
NM_001195139.2:c.1752+72C= NP_001182068.2:n.1752+72C=
NM_001365426.1:c.1401+72C= NP_001352355.1:n.1401+72C=
NR_158212.1:n.1786+72C=