Canonical Allele Identifier: CA2807523808
Gene: COG4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.70484351T>C , CM000678.2:g.70484351T>C GRCh38
NC_000016.9:g.70518254T>C , CM000678.1:g.70518254T>C GRCh37
NC_000016.8:g.69075755T>C NCBI36
NG_027529.1:g.44204A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000534772.2:c.*1787-382A>G ENSP00000461912.2:n.*1787-382A>G
ENST00000703106.1:c.1660-286A>G ENSP00000515173.1:n.1660-286A>G
ENST00000703107.1:c.*1640-382A>G ENSP00000515174.1:n.*1640-382A>G
ENST00000703108.1:c.*159-382A>G ENSP00000515175.1:n.*159-382A>G
ENST00000703109.1:c.1744-382A>G ENSP00000515176.1:n.1744-382A>G
ENST00000703110.1:c.*1213-382A>G ENSP00000515177.1:n.*1213-382A>G
ENST00000703111.1:n.1718-382A>G
ENST00000703112.1:n.2484-382A>G
ENST00000703113.1:c.*1124-382A>G ENSP00000515178.1:n.*1124-382A>G
ENST00000703114.1:c.*360-382A>G ENSP00000515179.1:n.*360-382A>G
ENST00000703115.1:c.824-382A>G ENSP00000515180.1:n.824-382A>G
ENST00000323786.10:c.1711-382A>G MANE Select ENSP00000315775.5:n.1711-382A>G
ENST00000564415.6:c.*1491-382A>G ENSP00000456653.2:n.*1491-382A>G
ENST00000674443.1:c.1636-382A>G ENSP00000501405.1:n.1636-382A>G
ENST00000323786.9:c.1711-382A>G ENSP00000315775.5:n.1711-382A>G
ENST00000393612.8:c.1648-382A>G ENSP00000377236.5:n.1648-382A>G
ENST00000482252.5:c.1858-382A>G ENSP00000432802.1:n.1858-382A>G
ENST00000526700.5:n.887-382A>G
ENST00000530314.5:n.2390-382A>G
ENST00000564315.1:n.171-382A>G
ENST00000564415.5:c.*1491-382A>G ENSP00000456653.1:n.*1491-382A>G
NM_001195139.1:c.1648-382A>G NP_001182068.1:n.1648-382A>G
NM_015386.2:c.1711-382A>G NP_056201.2:n.1711-382A>G
XM_011522981.1:c.1285-382A>G XP_011521283.1:n.1285-382A>G
XR_933266.1:n.1657-382A>G
XR_933267.1:n.1657-382A>G
XM_011522981.3:c.1285-382A>G XP_011521283.1:n.1285-382A>G
XM_024450224.1:c.730-382A>G XP_024305992.1:n.730-382A>G
XR_001751889.1:n.1594-382A>G
XR_933266.2:n.1657-382A>G
NM_015386.3:c.1711-382A>G MANE Select NP_056201.2:n.1711-382A>G
NM_001195139.2:c.1636-382A>G NP_001182068.2:n.1636-382A>G
NM_001365426.1:c.1285-382A>G NP_001352355.1:n.1285-382A>G
NR_158212.1:n.1670-382A>G