Canonical Allele Identifier: CA396580572

Gene: COG4

Linked Data

• MyVariant Identifiers: chr16:g.70517756C>A (hg19) ; chr16:g.70483853C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70483853C>A , CM000678.2:g.70483853C>A	GRCh38
NC_000016.9:g.70517756C>A , CM000678.1:g.70517756C>A	GRCh37
NC_000016.8:g.69075257C>A	NCBI36
NG_027529.1:g.44702G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534772.2:c.*1903G>T	ENSP00000461912.2:n.*1903G>T
ENST00000703106.1:c.1872G>T	ENSP00000515173.1:n.1872G>T
ENST00000703107.1:c.*1756G>T	ENSP00000515174.1:n.*1756G>T
ENST00000703108.1:c.*275G>T	ENSP00000515175.1:n.*275G>T
ENST00000703109.1:c.1860G>T	ENSP00000515176.1:p.Gln620His
ENST00000703110.1:c.*1329G>T	ENSP00000515177.1:n.*1329G>T
ENST00000703111.1:n.1834G>T
ENST00000703112.1:n.2600G>T
ENST00000703113.1:c.*1240G>T	ENSP00000515178.1:n.*1240G>T
ENST00000703114.1:c.*476G>T	ENSP00000515179.1:n.*476G>T
ENST00000703115.1:c.940G>T	ENSP00000515180.1:n.940G>T
ENST00000323786.10:c.1827G>T MANE Select	ENSP00000315775.5:p.Gln609His
ENST00000564415.6:c.*1607G>T	ENSP00000456653.2:n.*1607G>T
ENST00000674443.1:c.1752G>T	ENSP00000501405.1:p.Gln584His
ENST00000323786.9:c.1827G>T	ENSP00000315775.5:p.Gln609His
ENST00000393612.8:c.1764G>T	ENSP00000377236.5:p.Gln588His
ENST00000482252.5:c.1974G>T	ENSP00000432802.1:n.1974G>T
ENST00000526700.5:n.1003G>T
ENST00000530314.5:n.2506G>T
ENST00000564315.1:n.287G>T
ENST00000564415.5:c.*1607G>T	ENSP00000456653.1:n.*1607G>T
NM_001195139.1:c.1764G>T	NP_001182068.1:p.Gln588His
NM_015386.2:c.1827G>T	NP_056201.2:p.Gln609His
XM_011522981.1:c.1401G>T	XP_011521283.1:p.Gln467His
XR_933266.1:n.1773G>T
XR_933267.1:n.1773G>T
XM_011522981.3:c.1401G>T	XP_011521283.1:p.Gln467His
XM_024450224.1:c.846G>T	XP_024305992.1:p.Gln282His
XR_001751889.1:n.1710G>T
XR_933266.2:n.1773G>T
NM_015386.3:c.1827G>T MANE Select	NP_056201.2:p.Gln609His
NM_001195139.2:c.1752G>T	NP_001182068.2:p.Gln584His
NM_001365426.1:c.1401G>T	NP_001352355.1:p.Gln467His
NR_158212.1:n.1786G>T