Canonical Allele Identifier: CA2634068331

Gene: COG4

Linked Data

• gnomAD v4: 16-70483755-GTCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70483760_70483762del , CM000678.2:g.70483760_70483762del	GRCh38
NC_000016.9:g.70517663_70517665del , CM000678.1:g.70517663_70517665del	GRCh37
NC_000016.8:g.69075164_69075166del	NCBI36
NG_027529.1:g.44797_44799del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534772.2:c.*1903+95_*1903+97del	ENSP00000461912.2:n.*1903+95_*1903+97del
ENST00000703106.1:c.1872+95_1872+97del	ENSP00000515173.1:n.1872+95_1872+97del
ENST00000703107.1:c.*1756+95_*1756+97del	ENSP00000515174.1:n.*1756+95_*1756+97del
ENST00000703108.1:c.*275+95_*275+97del	ENSP00000515175.1:n.*275+95_*275+97del
ENST00000703109.1:c.1860+95_1860+97del	ENSP00000515176.1:n.1860+95_1860+97del
ENST00000703110.1:c.*1329+95_*1329+97del	ENSP00000515177.1:n.*1329+95_*1329+97del
ENST00000703111.1:n.1834+95_1834+97del
ENST00000703112.1:n.2600+95_2600+97del
ENST00000703113.1:c.*1240+95_*1240+97del	ENSP00000515178.1:n.*1240+95_*1240+97del
ENST00000703114.1:c.*476+95_*476+97del	ENSP00000515179.1:n.*476+95_*476+97del
ENST00000703115.1:c.940+95_940+97del	ENSP00000515180.1:n.940+95_940+97del
ENST00000323786.10:c.1827+95_1827+97del MANE Select	ENSP00000315775.5:n.1827+95_1827+97del
ENST00000564415.6:c.*1607+95_*1607+97del	ENSP00000456653.2:n.*1607+95_*1607+97del
ENST00000674443.1:c.1752+95_1752+97del	ENSP00000501405.1:n.1752+95_1752+97del
ENST00000323786.9:c.1827+95_1827+97del	ENSP00000315775.5:n.1827+95_1827+97del
ENST00000393612.8:c.1764+95_1764+97del	ENSP00000377236.5:n.1764+95_1764+97del
ENST00000482252.5:c.1974+95_1974+97del	ENSP00000432802.1:n.1974+95_1974+97del
ENST00000526700.5:n.1003+95_1003+97del
ENST00000530314.5:n.2506+95_2506+97del
ENST00000564315.1:n.287+95_287+97del
ENST00000564415.5:c.*1607+95_*1607+97del	ENSP00000456653.1:n.*1607+95_*1607+97del
NM_001195139.1:c.1764+95_1764+97del	NP_001182068.1:n.1764+95_1764+97del
NM_015386.2:c.1827+95_1827+97del	NP_056201.2:n.1827+95_1827+97del
XM_011522981.1:c.1401+95_1401+97del	XP_011521283.1:n.1401+95_1401+97del
XR_933266.1:n.1773+95_1773+97del
XR_933267.1:n.1773+95_1773+97del
XM_011522981.3:c.1401+95_1401+97del	XP_011521283.1:n.1401+95_1401+97del
XM_024450224.1:c.846+95_846+97del	XP_024305992.1:n.846+95_846+97del
XR_001751889.1:n.1710+95_1710+97del
XR_933266.2:n.1773+95_1773+97del
NM_015386.3:c.1827+95_1827+97del MANE Select	NP_056201.2:n.1827+95_1827+97del
NM_001195139.2:c.1752+95_1752+97del	NP_001182068.2:n.1752+95_1752+97del
NM_001365426.1:c.1401+95_1401+97del	NP_001352355.1:n.1401+95_1401+97del
NR_158212.1:n.1786+95_1786+97del