Canonical Allele Identifier: CA1105604159

Gene: COG5

Linked Data

• gnomAD v3: 7-107297807-AT-A
• gnomAD v4: 7-107297807-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107297808del , CM000669.2:g.107297808del	GRCh38
NC_000007.13:g.106938253del , CM000669.1:g.106938253del	GRCh37
NC_000007.12:g.106725489del	NCBI36
NG_028095.1:g.271707del
NG_028095.2:g.271707del

Transcript Alleles

HGVS	Amino-acid change
ENST00000297135.9:c.1313+334del MANE Select	ENSP00000297135.4:n.1313+334del
ENST00000347053.8:c.1313+334del	ENSP00000334703.3:n.1313+334del
ENST00000393603.7:c.1313+334del	ENSP00000377228.3:n.1313+334del
ENST00000297135.7:c.1406+334del	ENSP00000297135.3:n.1406+334del
ENST00000347053.7:c.1406+334del	ENSP00000334703.2:n.1406+334del
ENST00000393603.6:c.1406+334del	ENSP00000377228.2:n.1406+334del
NM_001161520.1:c.1406+334del	NP_001154992.1:n.1406+334del
NM_006348.3:c.1406+334del	NP_006339.3:n.1406+334del
NM_181733.2:c.1406+334del	NP_859422.2:n.1406+334del
XM_011515738.1:c.1406+334del	XP_011514040.1:n.1406+334del
XM_024446634.1:c.1406+334del	XP_024302402.1:n.1406+334del
NM_001161520.2:c.1313+334del	NP_001154992.2:n.1313+334del
NM_006348.4:c.1313+334del	NP_006339.4:n.1313+334del
NM_181733.3:c.1313+334del	NP_859422.3:n.1313+334del
NM_001379511.1:c.1313+334del	NP_001366440.1:n.1313+334del
NM_001379512.1:c.1313+334del	NP_001366441.1:n.1313+334del
NM_001379513.1:c.1313+334del	NP_001366442.1:n.1313+334del
NM_001379514.1:c.1313+334del	NP_001366443.1:n.1313+334del
NM_001379515.1:c.743+334del	NP_001366444.1:n.743+334del
NM_001379516.1:c.599+334del	NP_001366445.1:n.599+334del
NM_006348.5:c.1313+334del MANE Select	NP_006339.4:n.1313+334del
NM_181733.4:c.1313+334del	NP_859422.3:n.1313+334del