Canonical Allele Identifier: CA496227822

Gene: COG4

Linked Data

• MyVariant Identifiers: chr16:g.70515358C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70481455C>T , CM000678.2:g.70481455C>T	GRCh38
NC_000016.9:g.70515358C>T , CM000678.1:g.70515358C>T	GRCh37
NC_000016.8:g.69072859C>T	NCBI36
NG_027529.1:g.47100G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534772.2:c.*2215G>A	ENSP00000461912.2:n.*2215G>A
ENST00000703106.1:c.2184G>A	ENSP00000515173.1:n.2184G>A
ENST00000703107.1:c.*2068G>A	ENSP00000515174.1:n.*2068G>A
ENST00000703108.1:c.*587G>A	ENSP00000515175.1:n.*587G>A
ENST00000703109.1:c.2172G>A	ENSP00000515176.1:p.Arg724=
ENST00000703110.1:c.*1641G>A	ENSP00000515177.1:n.*1641G>A
ENST00000703111.1:n.2422G>A
ENST00000703112.1:n.3083G>A
ENST00000703113.1:c.*1552G>A	ENSP00000515178.1:n.*1552G>A
ENST00000703114.1:c.*788G>A	ENSP00000515179.1:n.*788G>A
ENST00000703115.1:c.1252G>A	ENSP00000515180.1:n.1252G>A
ENST00000323786.10:c.2139G>A MANE Select	ENSP00000315775.5:p.Arg713=
ENST00000564415.6:c.*1919G>A	ENSP00000456653.2:n.*1919G>A
ENST00000674443.1:c.2064G>A	ENSP00000501405.1:p.Arg688=
ENST00000323786.9:c.2139G>A	ENSP00000315775.5:p.Arg713=
ENST00000393612.8:c.2076G>A	ENSP00000377236.5:p.Arg692=
ENST00000482252.5:c.2286G>A	ENSP00000432802.1:n.2286G>A
ENST00000526700.5:n.1315G>A
ENST00000530314.5:n.2818G>A
ENST00000564415.5:c.*1919G>A	ENSP00000456653.1:n.*1919G>A
ENST00000565715.1:c.201G>A	ENSP00000455693.1:p.Arg67=
NM_001195139.1:c.2076G>A	NP_001182068.1:p.Arg692=
NM_015386.2:c.2139G>A	NP_056201.2:p.Arg713=
XM_011522981.1:c.1713G>A	XP_011521283.1:p.Arg571=
XM_011522981.3:c.1713G>A	XP_011521283.1:p.Arg571=
XM_024450224.1:c.1158G>A	XP_024305992.1:p.Arg386=
XR_933266.2:n.2085G>A
NM_015386.3:c.2139G>A MANE Select	NP_056201.2:p.Arg713=
NM_001195139.2:c.2064G>A	NP_001182068.2:p.Arg688=
NM_001365426.1:c.1713G>A	NP_001352355.1:p.Arg571=
NR_158212.1:n.2098G>A