Canonical Allele Identifier: CA2230762819

Gene: COG4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70483831A= , CM000678.2:g.70483831A=	GRCh38
NC_000016.9:g.70517734A= , CM000678.1:g.70517734A=	GRCh37
NC_000016.8:g.69075235A=	NCBI36
NG_027529.1:g.44724T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534772.2:c.*1903+22T=	ENSP00000461912.2:n.*1903+22T=
ENST00000703106.1:c.1872+22T=	ENSP00000515173.1:n.1872+22T=
ENST00000703107.1:c.*1756+22T=	ENSP00000515174.1:n.*1756+22T=
ENST00000703108.1:c.*275+22T=	ENSP00000515175.1:n.*275+22T=
ENST00000703109.1:c.1860+22T=	ENSP00000515176.1:n.1860+22T=
ENST00000703110.1:c.*1329+22T=	ENSP00000515177.1:n.*1329+22T=
ENST00000703111.1:n.1834+22T=
ENST00000703112.1:n.2600+22T=
ENST00000703113.1:c.*1240+22T=	ENSP00000515178.1:n.*1240+22T=
ENST00000703114.1:c.*476+22T=	ENSP00000515179.1:n.*476+22T=
ENST00000703115.1:c.940+22T=	ENSP00000515180.1:n.940+22T=
ENST00000323786.10:c.1827+22T= MANE Select	ENSP00000315775.5:n.1827+22T=
ENST00000564415.6:c.*1607+22T=	ENSP00000456653.2:n.*1607+22T=
ENST00000674443.1:c.1752+22T=	ENSP00000501405.1:n.1752+22T=
ENST00000323786.9:c.1827+22T=	ENSP00000315775.5:n.1827+22T=
ENST00000393612.8:c.1764+22T=	ENSP00000377236.5:n.1764+22T=
ENST00000482252.5:c.1974+22T=	ENSP00000432802.1:n.1974+22T=
ENST00000526700.5:n.1003+22T=
ENST00000530314.5:n.2506+22T=
ENST00000564315.1:n.287+22T=
ENST00000564415.5:c.*1607+22T=	ENSP00000456653.1:n.*1607+22T=
NM_001195139.1:c.1764+22T=	NP_001182068.1:n.1764+22T=
NM_015386.2:c.1827+22T=	NP_056201.2:n.1827+22T=
XM_011522981.1:c.1401+22T=	XP_011521283.1:n.1401+22T=
XR_933266.1:n.1773+22T=
XR_933267.1:n.1773+22T=
XM_011522981.3:c.1401+22T=	XP_011521283.1:n.1401+22T=
XM_024450224.1:c.846+22T=	XP_024305992.1:n.846+22T=
XR_001751889.1:n.1710+22T=
XR_933266.2:n.1773+22T=
NM_015386.3:c.1827+22T= MANE Select	NP_056201.2:n.1827+22T=
NM_001195139.2:c.1752+22T=	NP_001182068.2:n.1752+22T=
NM_001365426.1:c.1401+22T=	NP_001352355.1:n.1401+22T=
NR_158212.1:n.1786+22T=