Canonical Allele Identifier: CA2230785037

Gene: COG4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70481484C= , CM000678.2:g.70481484C=	GRCh38
NC_000016.9:g.70515387C= , CM000678.1:g.70515387C=	GRCh37
NC_000016.8:g.69072888C=	NCBI36
NG_027529.1:g.47071G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534772.2:c.*2186G=	ENSP00000461912.2:n.*2186G=
ENST00000703106.1:c.2155G=	ENSP00000515173.1:n.2155G=
ENST00000703107.1:c.*2039G=	ENSP00000515174.1:n.*2039G=
ENST00000703108.1:c.*558G=	ENSP00000515175.1:n.*558G=
ENST00000703109.1:c.2143G=	ENSP00000515176.1:p.Gly715=
ENST00000703110.1:c.*1612G=	ENSP00000515177.1:n.*1612G=
ENST00000703111.1:n.2393G=
ENST00000703112.1:n.3054G=
ENST00000703113.1:c.*1523G=	ENSP00000515178.1:n.*1523G=
ENST00000703114.1:c.*759G=	ENSP00000515179.1:n.*759G=
ENST00000703115.1:c.1223G=	ENSP00000515180.1:n.1223G=
ENST00000323786.10:c.2110G= MANE Select	ENSP00000315775.5:p.Gly704=
ENST00000564415.6:c.*1890G=	ENSP00000456653.2:n.*1890G=
ENST00000674443.1:c.2035G=	ENSP00000501405.1:p.Gly679=
ENST00000323786.9:c.2110G=	ENSP00000315775.5:p.Gly704=
ENST00000393612.8:c.2047G=	ENSP00000377236.5:p.Gly683=
ENST00000482252.5:c.2257G=	ENSP00000432802.1:n.2257G=
ENST00000526700.5:n.1286G=
ENST00000530314.5:n.2789G=
ENST00000564415.5:c.*1890G=	ENSP00000456653.1:n.*1890G=
ENST00000565715.1:c.172G=	ENSP00000455693.1:p.Gly58=
NM_001195139.1:c.2047G=	NP_001182068.1:p.Gly683=
NM_015386.2:c.2110G=	NP_056201.2:p.Gly704=
XM_011522981.1:c.1684G=	XP_011521283.1:p.Gly562=
XM_011522981.3:c.1684G=	XP_011521283.1:p.Gly562=
XM_024450224.1:c.1129G=	XP_024305992.1:p.Gly377=
XR_001751889.1:n.1993G=
XR_933266.2:n.2056G=
NM_015386.3:c.2110G= MANE Select	NP_056201.2:p.Gly704=
NM_001195139.2:c.2035G=	NP_001182068.2:p.Gly679=
NM_001365426.1:c.1684G=	NP_001352355.1:p.Gly562=
NR_158212.1:n.2069G=