Canonical Allele Identifier: CA2634068934

Gene: COG4

Linked Data

• gnomAD v4: 16-70484113-TGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70484114_70484115del , CM000678.2:g.70484114_70484115del	GRCh38
NC_000016.9:g.70518017_70518018del , CM000678.1:g.70518017_70518018del	GRCh37
NC_000016.8:g.69075518_69075519del	NCBI36
NG_027529.1:g.44440_44441del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534772.2:c.*1787-146_*1787-145del	ENSP00000461912.2:n.*1787-146_*1787-145del
ENST00000703106.1:c.1660-50_1660-49del	ENSP00000515173.1:n.1660-50_1660-49del
ENST00000703107.1:c.*1640-146_*1640-145del	ENSP00000515174.1:n.*1640-146_*1640-145del
ENST00000703108.1:c.*159-146_*159-145del	ENSP00000515175.1:n.*159-146_*159-145del
ENST00000703109.1:c.1744-146_1744-145del	ENSP00000515176.1:n.1744-146_1744-145del
ENST00000703110.1:c.*1213-146_*1213-145del	ENSP00000515177.1:n.*1213-146_*1213-145del
ENST00000703111.1:n.1718-146_1718-145del
ENST00000703112.1:n.2484-146_2484-145del
ENST00000703113.1:c.*1124-146_*1124-145del	ENSP00000515178.1:n.*1124-146_*1124-145del
ENST00000703114.1:c.*360-146_*360-145del	ENSP00000515179.1:n.*360-146_*360-145del
ENST00000703115.1:c.824-146_824-145del	ENSP00000515180.1:n.824-146_824-145del
ENST00000323786.10:c.1711-146_1711-145del MANE Select	ENSP00000315775.5:n.1711-146_1711-145del
ENST00000564415.6:c.*1491-146_*1491-145del	ENSP00000456653.2:n.*1491-146_*1491-145del
ENST00000674443.1:c.1636-146_1636-145del	ENSP00000501405.1:n.1636-146_1636-145del
ENST00000323786.9:c.1711-146_1711-145del	ENSP00000315775.5:n.1711-146_1711-145del
ENST00000393612.8:c.1648-146_1648-145del	ENSP00000377236.5:n.1648-146_1648-145del
ENST00000482252.5:c.1858-146_1858-145del	ENSP00000432802.1:n.1858-146_1858-145del
ENST00000526700.5:n.887-146_887-145del
ENST00000530314.5:n.2390-146_2390-145del
ENST00000564315.1:n.171-146_171-145del
ENST00000564415.5:c.*1491-146_*1491-145del	ENSP00000456653.1:n.*1491-146_*1491-145del
NM_001195139.1:c.1648-146_1648-145del	NP_001182068.1:n.1648-146_1648-145del
NM_015386.2:c.1711-146_1711-145del	NP_056201.2:n.1711-146_1711-145del
XM_011522981.1:c.1285-146_1285-145del	XP_011521283.1:n.1285-146_1285-145del
XR_933266.1:n.1657-146_1657-145del
XR_933267.1:n.1657-146_1657-145del
XM_011522981.3:c.1285-146_1285-145del	XP_011521283.1:n.1285-146_1285-145del
XM_024450224.1:c.730-146_730-145del	XP_024305992.1:n.730-146_730-145del
XR_001751889.1:n.1594-146_1594-145del
XR_933266.2:n.1657-146_1657-145del
NM_015386.3:c.1711-146_1711-145del MANE Select	NP_056201.2:n.1711-146_1711-145del
NM_001195139.2:c.1636-146_1636-145del	NP_001182068.2:n.1636-146_1636-145del
NM_001365426.1:c.1285-146_1285-145del	NP_001352355.1:n.1285-146_1285-145del
NR_158212.1:n.1670-146_1670-145del