Canonical Allele Identifier: CA2230762780
Gene: COG4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.70483778G= , CM000678.2:g.70483778G= GRCh38
NC_000016.9:g.70517681G= , CM000678.1:g.70517681G= GRCh37
NC_000016.8:g.69075182G= NCBI36
NG_027529.1:g.44777C=

Transcript Alleles

HGVS Amino-acid change
ENST00000534772.2:c.*1903+75C= ENSP00000461912.2:n.*1903+75C=
ENST00000703106.1:c.1872+75C= ENSP00000515173.1:n.1872+75C=
ENST00000703107.1:c.*1756+75C= ENSP00000515174.1:n.*1756+75C=
ENST00000703108.1:c.*275+75C= ENSP00000515175.1:n.*275+75C=
ENST00000703109.1:c.1860+75C= ENSP00000515176.1:n.1860+75C=
ENST00000703110.1:c.*1329+75C= ENSP00000515177.1:n.*1329+75C=
ENST00000703111.1:n.1834+75C=
ENST00000703112.1:n.2600+75C=
ENST00000703113.1:c.*1240+75C= ENSP00000515178.1:n.*1240+75C=
ENST00000703114.1:c.*476+75C= ENSP00000515179.1:n.*476+75C=
ENST00000703115.1:c.940+75C= ENSP00000515180.1:n.940+75C=
ENST00000323786.10:c.1827+75C= MANE Select ENSP00000315775.5:n.1827+75C=
ENST00000564415.6:c.*1607+75C= ENSP00000456653.2:n.*1607+75C=
ENST00000674443.1:c.1752+75C= ENSP00000501405.1:n.1752+75C=
ENST00000323786.9:c.1827+75C= ENSP00000315775.5:n.1827+75C=
ENST00000393612.8:c.1764+75C= ENSP00000377236.5:n.1764+75C=
ENST00000482252.5:c.1974+75C= ENSP00000432802.1:n.1974+75C=
ENST00000526700.5:n.1003+75C=
ENST00000530314.5:n.2506+75C=
ENST00000564315.1:n.287+75C=
ENST00000564415.5:c.*1607+75C= ENSP00000456653.1:n.*1607+75C=
NM_001195139.1:c.1764+75C= NP_001182068.1:n.1764+75C=
NM_015386.2:c.1827+75C= NP_056201.2:n.1827+75C=
XM_011522981.1:c.1401+75C= XP_011521283.1:n.1401+75C=
XR_933266.1:n.1773+75C=
XR_933267.1:n.1773+75C=
XM_011522981.3:c.1401+75C= XP_011521283.1:n.1401+75C=
XM_024450224.1:c.846+75C= XP_024305992.1:n.846+75C=
XR_001751889.1:n.1710+75C=
XR_933266.2:n.1773+75C=
NM_015386.3:c.1827+75C= MANE Select NP_056201.2:n.1827+75C=
NM_001195139.2:c.1752+75C= NP_001182068.2:n.1752+75C=
NM_001365426.1:c.1401+75C= NP_001352355.1:n.1401+75C=
NR_158212.1:n.1786+75C=