Canonical Allele Identifier: CA2230762789
Gene: COG4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.70483787_70483788delinsGC , CM000678.2:g.70483787_70483788delinsGC GRCh38
NC_000016.9:g.70517690_70517691delinsGC , CM000678.1:g.70517690_70517691delinsGC GRCh37
NC_000016.8:g.69075191_69075192delinsGC NCBI36
NG_027529.1:g.44767_44768delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000534772.2:c.*1903+65_*1903+66delinsGC ENSP00000461912.2:n.*1903+65_*1903+66deli...
ENST00000703106.1:c.1872+65_1872+66delinsGC ENSP00000515173.1:n.1872+65_1872+66delins...
ENST00000703107.1:c.*1756+65_*1756+66delinsGC ENSP00000515174.1:n.*1756+65_*1756+66deli...
ENST00000703108.1:c.*275+65_*275+66delinsGC ENSP00000515175.1:n.*275+65_*275+66delins...
ENST00000703109.1:c.1860+65_1860+66delinsGC ENSP00000515176.1:n.1860+65_1860+66delins...
ENST00000703110.1:c.*1329+65_*1329+66delinsGC ENSP00000515177.1:n.*1329+65_*1329+66deli...
ENST00000703111.1:n.1834+65_1834+66delinsGC
ENST00000703112.1:n.2600+65_2600+66delinsGC
ENST00000703113.1:c.*1240+65_*1240+66delinsGC ENSP00000515178.1:n.*1240+65_*1240+66deli...
ENST00000703114.1:c.*476+65_*476+66delinsGC ENSP00000515179.1:n.*476+65_*476+66delins...
ENST00000703115.1:c.940+65_940+66delinsGC ENSP00000515180.1:n.940+65_940+66delinsGC...
ENST00000323786.10:c.1827+65_1827+66delinsGC MANE Select ENSP00000315775.5:n.1827+65_1827+66delins...
ENST00000564415.6:c.*1607+65_*1607+66delinsGC ENSP00000456653.2:n.*1607+65_*1607+66deli...
ENST00000674443.1:c.1752+65_1752+66delinsGC ENSP00000501405.1:n.1752+65_1752+66delins...
ENST00000323786.9:c.1827+65_1827+66delinsGC ENSP00000315775.5:n.1827+65_1827+66delins...
ENST00000393612.8:c.1764+65_1764+66delinsGC ENSP00000377236.5:n.1764+65_1764+66delins...
ENST00000482252.5:c.1974+65_1974+66delinsGC ENSP00000432802.1:n.1974+65_1974+66delins...
ENST00000526700.5:n.1003+65_1003+66delinsGC
ENST00000530314.5:n.2506+65_2506+66delinsGC
ENST00000564315.1:n.287+65_287+66delinsGC
ENST00000564415.5:c.*1607+65_*1607+66delinsGC ENSP00000456653.1:n.*1607+65_*1607+66deli...
NM_001195139.1:c.1764+65_1764+66delinsGC NP_001182068.1:n.1764+65_1764+66delinsGC
NM_015386.2:c.1827+65_1827+66delinsGC NP_056201.2:n.1827+65_1827+66delinsGC
XM_011522981.1:c.1401+65_1401+66delinsGC XP_011521283.1:n.1401+65_1401+66delinsGC
XR_933266.1:n.1773+65_1773+66delinsGC
XR_933267.1:n.1773+65_1773+66delinsGC
XM_011522981.3:c.1401+65_1401+66delinsGC XP_011521283.1:n.1401+65_1401+66delinsGC
XM_024450224.1:c.846+65_846+66delinsGC XP_024305992.1:n.846+65_846+66delinsGC
XR_001751889.1:n.1710+65_1710+66delinsGC
XR_933266.2:n.1773+65_1773+66delinsGC
NM_015386.3:c.1827+65_1827+66delinsGC MANE Select NP_056201.2:n.1827+65_1827+66delinsGC
NM_001195139.2:c.1752+65_1752+66delinsGC NP_001182068.2:n.1752+65_1752+66delinsGC
NM_001365426.1:c.1401+65_1401+66delinsGC NP_001352355.1:n.1401+65_1401+66delinsGC
NR_158212.1:n.1786+65_1786+66delinsGC