Canonical Allele Identifier: CA2634068439

Gene: COG4

Linked Data

• gnomAD v4: 16-70483794-ATCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70483798_70483800del , CM000678.2:g.70483798_70483800del	GRCh38
NC_000016.9:g.70517701_70517703del , CM000678.1:g.70517701_70517703del	GRCh37
NC_000016.8:g.69075202_69075204del	NCBI36
NG_027529.1:g.44758_44760del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534772.2:c.*1903+56_*1903+58del	ENSP00000461912.2:n.*1903+56_*1903+58del
ENST00000703106.1:c.1872+56_1872+58del	ENSP00000515173.1:n.1872+56_1872+58del
ENST00000703107.1:c.*1756+56_*1756+58del	ENSP00000515174.1:n.*1756+56_*1756+58del
ENST00000703108.1:c.*275+56_*275+58del	ENSP00000515175.1:n.*275+56_*275+58del
ENST00000703109.1:c.1860+56_1860+58del	ENSP00000515176.1:n.1860+56_1860+58del
ENST00000703110.1:c.*1329+56_*1329+58del	ENSP00000515177.1:n.*1329+56_*1329+58del
ENST00000703111.1:n.1834+56_1834+58del
ENST00000703112.1:n.2600+56_2600+58del
ENST00000703113.1:c.*1240+56_*1240+58del	ENSP00000515178.1:n.*1240+56_*1240+58del
ENST00000703114.1:c.*476+56_*476+58del	ENSP00000515179.1:n.*476+56_*476+58del
ENST00000703115.1:c.940+56_940+58del	ENSP00000515180.1:n.940+56_940+58del
ENST00000323786.10:c.1827+56_1827+58del MANE Select	ENSP00000315775.5:n.1827+56_1827+58del
ENST00000564415.6:c.*1607+56_*1607+58del	ENSP00000456653.2:n.*1607+56_*1607+58del
ENST00000674443.1:c.1752+56_1752+58del	ENSP00000501405.1:n.1752+56_1752+58del
ENST00000323786.9:c.1827+56_1827+58del	ENSP00000315775.5:n.1827+56_1827+58del
ENST00000393612.8:c.1764+56_1764+58del	ENSP00000377236.5:n.1764+56_1764+58del
ENST00000482252.5:c.1974+56_1974+58del	ENSP00000432802.1:n.1974+56_1974+58del
ENST00000526700.5:n.1003+56_1003+58del
ENST00000530314.5:n.2506+56_2506+58del
ENST00000564315.1:n.287+56_287+58del
ENST00000564415.5:c.*1607+56_*1607+58del	ENSP00000456653.1:n.*1607+56_*1607+58del
NM_001195139.1:c.1764+56_1764+58del	NP_001182068.1:n.1764+56_1764+58del
NM_015386.2:c.1827+56_1827+58del	NP_056201.2:n.1827+56_1827+58del
XM_011522981.1:c.1401+56_1401+58del	XP_011521283.1:n.1401+56_1401+58del
XR_933266.1:n.1773+56_1773+58del
XR_933267.1:n.1773+56_1773+58del
XM_011522981.3:c.1401+56_1401+58del	XP_011521283.1:n.1401+56_1401+58del
XM_024450224.1:c.846+56_846+58del	XP_024305992.1:n.846+56_846+58del
XR_001751889.1:n.1710+56_1710+58del
XR_933266.2:n.1773+56_1773+58del
NM_015386.3:c.1827+56_1827+58del MANE Select	NP_056201.2:n.1827+56_1827+58del
NM_001195139.2:c.1752+56_1752+58del	NP_001182068.2:n.1752+56_1752+58del
NM_001365426.1:c.1401+56_1401+58del	NP_001352355.1:n.1401+56_1401+58del
NR_158212.1:n.1786+56_1786+58del