Canonical Allele Identifier: CA396578387

Gene: COG4

Linked Data

• MyVariant Identifiers: chr16:g.70515351T>A (hg19) ; chr16:g.70481448T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70481448T>A , CM000678.2:g.70481448T>A	GRCh38
NC_000016.9:g.70515351T>A , CM000678.1:g.70515351T>A	GRCh37
NC_000016.8:g.69072852T>A	NCBI36
NG_027529.1:g.47107A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534772.2:c.*2222A>T	ENSP00000461912.2:n.*2222A>T
ENST00000703106.1:c.2191A>T	ENSP00000515173.1:n.2191A>T
ENST00000703107.1:c.*2075A>T	ENSP00000515174.1:n.*2075A>T
ENST00000703108.1:c.*594A>T	ENSP00000515175.1:n.*594A>T
ENST00000703109.1:c.2179A>T	ENSP00000515176.1:p.Ile727Phe
ENST00000703110.1:c.*1648A>T	ENSP00000515177.1:n.*1648A>T
ENST00000703111.1:n.2429A>T
ENST00000703112.1:n.3090A>T
ENST00000703113.1:c.*1559A>T	ENSP00000515178.1:n.*1559A>T
ENST00000703114.1:c.*795A>T	ENSP00000515179.1:n.*795A>T
ENST00000703115.1:c.1259A>T	ENSP00000515180.1:n.1259A>T
ENST00000323786.10:c.2146A>T MANE Select	ENSP00000315775.5:p.Ile716Phe
ENST00000564415.6:c.*1926A>T	ENSP00000456653.2:n.*1926A>T
ENST00000674443.1:c.2071A>T	ENSP00000501405.1:p.Ile691Phe
ENST00000323786.9:c.2146A>T	ENSP00000315775.5:p.Ile716Phe
ENST00000393612.8:c.2083A>T	ENSP00000377236.5:p.Ile695Phe
ENST00000482252.5:c.2293A>T	ENSP00000432802.1:n.2293A>T
ENST00000526700.5:n.1322A>T
ENST00000530314.5:n.2825A>T
ENST00000564415.5:c.*1926A>T	ENSP00000456653.1:n.*1926A>T
ENST00000565715.1:c.208A>T	ENSP00000455693.1:p.Ile70Phe
NM_001195139.1:c.2083A>T	NP_001182068.1:p.Ile695Phe
NM_015386.2:c.2146A>T	NP_056201.2:p.Ile716Phe
XM_011522981.1:c.1720A>T	XP_011521283.1:p.Ile574Phe
XM_011522981.3:c.1720A>T	XP_011521283.1:p.Ile574Phe
XM_024450224.1:c.1165A>T	XP_024305992.1:p.Ile389Phe
XR_933266.2:n.2092A>T
NM_015386.3:c.2146A>T MANE Select	NP_056201.2:p.Ile716Phe
NM_001195139.2:c.2071A>T	NP_001182068.2:p.Ile691Phe
NM_001365426.1:c.1720A>T	NP_001352355.1:p.Ile574Phe
NR_158212.1:n.2105A>T