Canonical Allele Identifier: CA2230762993
Gene: COG4 HGNC NCBI

Linked Data

dbSNP Id: rs2049072649

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.70483977A>G , CM000678.2:g.70483977A>G GRCh38
NC_000016.9:g.70517880A>G , CM000678.1:g.70517880A>G GRCh37
NC_000016.8:g.69075381A>G NCBI36
NG_027529.1:g.44578T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000534772.2:c.*1787-8T>C ENSP00000461912.2:n.*1787-8T>C
ENST00000703106.1:c.1748T>C ENSP00000515173.1:p.Leu583Pro
ENST00000703107.1:c.*1640-8T>C ENSP00000515174.1:n.*1640-8T>C
ENST00000703108.1:c.*159-8T>C ENSP00000515175.1:n.*159-8T>C
ENST00000703109.1:c.1744-8T>C ENSP00000515176.1:n.1744-8T>C
ENST00000703110.1:c.*1213-8T>C ENSP00000515177.1:n.*1213-8T>C
ENST00000703111.1:n.1718-8T>C
ENST00000703112.1:n.2484-8T>C
ENST00000703113.1:c.*1124-8T>C ENSP00000515178.1:n.*1124-8T>C
ENST00000703114.1:c.*360-8T>C ENSP00000515179.1:n.*360-8T>C
ENST00000703115.1:c.824-8T>C ENSP00000515180.1:n.824-8T>C
ENST00000323786.10:c.1711-8T>C MANE Select ENSP00000315775.5:n.1711-8T>C
ENST00000564415.6:c.*1491-8T>C ENSP00000456653.2:n.*1491-8T>C
ENST00000674443.1:c.1636-8T>C ENSP00000501405.1:n.1636-8T>C
ENST00000323786.9:c.1711-8T>C ENSP00000315775.5:n.1711-8T>C
ENST00000393612.8:c.1648-8T>C ENSP00000377236.5:n.1648-8T>C
ENST00000482252.5:c.1858-8T>C ENSP00000432802.1:n.1858-8T>C
ENST00000526700.5:n.887-8T>C
ENST00000530314.5:n.2390-8T>C
ENST00000564315.1:n.171-8T>C
ENST00000564415.5:c.*1491-8T>C ENSP00000456653.1:n.*1491-8T>C
NM_001195139.1:c.1648-8T>C NP_001182068.1:n.1648-8T>C
NM_015386.2:c.1711-8T>C NP_056201.2:n.1711-8T>C
XM_011522981.1:c.1285-8T>C XP_011521283.1:n.1285-8T>C
XR_933266.1:n.1657-8T>C
XR_933267.1:n.1657-8T>C
XM_011522981.3:c.1285-8T>C XP_011521283.1:n.1285-8T>C
XM_024450224.1:c.730-8T>C XP_024305992.1:n.730-8T>C
XR_001751889.1:n.1594-8T>C
XR_933266.2:n.1657-8T>C
NM_015386.3:c.1711-8T>C MANE Select NP_056201.2:n.1711-8T>C
NM_001195139.2:c.1636-8T>C NP_001182068.2:n.1636-8T>C
NM_001365426.1:c.1285-8T>C NP_001352355.1:n.1285-8T>C
NR_158212.1:n.1670-8T>C