Canonical Allele Identifier: CA2230762933

Gene: COG4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70483932C= , CM000678.2:g.70483932C=	GRCh38
NC_000016.9:g.70517835C= , CM000678.1:g.70517835C=	GRCh37
NC_000016.8:g.69075336C=	NCBI36
NG_027529.1:g.44623G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534772.2:c.*1824G=	ENSP00000461912.2:n.*1824G=
ENST00000703106.1:c.1793G=	ENSP00000515173.1:n.1793G=
ENST00000703107.1:c.*1677G=	ENSP00000515174.1:n.*1677G=
ENST00000703108.1:c.*196G=	ENSP00000515175.1:n.*196G=
ENST00000703109.1:c.1781G=	ENSP00000515176.1:p.Gly594=
ENST00000703110.1:c.*1250G=	ENSP00000515177.1:n.*1250G=
ENST00000703111.1:n.1755G=
ENST00000703112.1:n.2521G=
ENST00000703113.1:c.*1161G=	ENSP00000515178.1:n.*1161G=
ENST00000703114.1:c.*397G=	ENSP00000515179.1:n.*397G=
ENST00000703115.1:c.861G=	ENSP00000515180.1:n.861G=
ENST00000323786.10:c.1748G= MANE Select	ENSP00000315775.5:p.Gly583=
ENST00000564415.6:c.*1528G=	ENSP00000456653.2:n.*1528G=
ENST00000674443.1:c.1673G=	ENSP00000501405.1:p.Gly558=
ENST00000323786.9:c.1748G=	ENSP00000315775.5:p.Gly583=
ENST00000393612.8:c.1685G=	ENSP00000377236.5:p.Gly562=
ENST00000482252.5:c.1895G=	ENSP00000432802.1:n.1895G=
ENST00000526700.5:n.924G=
ENST00000530314.5:n.2427G=
ENST00000564315.1:n.208G=
ENST00000564415.5:c.*1528G=	ENSP00000456653.1:n.*1528G=
NM_001195139.1:c.1685G=	NP_001182068.1:p.Gly562=
NM_015386.2:c.1748G=	NP_056201.2:p.Gly583=
XM_011522981.1:c.1322G=	XP_011521283.1:p.Gly441=
XR_933266.1:n.1694G=
XR_933267.1:n.1694G=
XM_011522981.3:c.1322G=	XP_011521283.1:p.Gly441=
XM_024450224.1:c.767G=	XP_024305992.1:p.Gly256=
XR_001751889.1:n.1631G=
XR_933266.2:n.1694G=
NM_015386.3:c.1748G= MANE Select	NP_056201.2:p.Gly583=
NM_001195139.2:c.1673G=	NP_001182068.2:p.Gly558=
NM_001365426.1:c.1322G=	NP_001352355.1:p.Gly441=
NR_158212.1:n.1707G=