Canonical Allele Identifier: CA496228668

Gene: COG4

Linked Data

• MyVariant Identifiers: chr16:g.70517780G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70483877G>T , CM000678.2:g.70483877G>T	GRCh38
NC_000016.9:g.70517780G>T , CM000678.1:g.70517780G>T	GRCh37
NC_000016.8:g.69075281G>T	NCBI36
NG_027529.1:g.44678C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534772.2:c.*1879C>A	ENSP00000461912.2:n.*1879C>A
ENST00000703106.1:c.1848C>A	ENSP00000515173.1:n.1848C>A
ENST00000703107.1:c.*1732C>A	ENSP00000515174.1:n.*1732C>A
ENST00000703108.1:c.*251C>A	ENSP00000515175.1:n.*251C>A
ENST00000703109.1:c.1836C>A	ENSP00000515176.1:p.Ser612=
ENST00000703110.1:c.*1305C>A	ENSP00000515177.1:n.*1305C>A
ENST00000703111.1:n.1810C>A
ENST00000703112.1:n.2576C>A
ENST00000703113.1:c.*1216C>A	ENSP00000515178.1:n.*1216C>A
ENST00000703114.1:c.*452C>A	ENSP00000515179.1:n.*452C>A
ENST00000703115.1:c.916C>A	ENSP00000515180.1:n.916C>A
ENST00000323786.10:c.1803C>A MANE Select	ENSP00000315775.5:p.Ser601=
ENST00000564415.6:c.*1583C>A	ENSP00000456653.2:n.*1583C>A
ENST00000674443.1:c.1728C>A	ENSP00000501405.1:p.Ser576=
ENST00000323786.9:c.1803C>A	ENSP00000315775.5:p.Ser601=
ENST00000393612.8:c.1740C>A	ENSP00000377236.5:p.Ser580=
ENST00000482252.5:c.1950C>A	ENSP00000432802.1:n.1950C>A
ENST00000526700.5:n.979C>A
ENST00000530314.5:n.2482C>A
ENST00000564315.1:n.263C>A
ENST00000564415.5:c.*1583C>A	ENSP00000456653.1:n.*1583C>A
NM_001195139.1:c.1740C>A	NP_001182068.1:p.Ser580=
NM_015386.2:c.1803C>A	NP_056201.2:p.Ser601=
XM_011522981.1:c.1377C>A	XP_011521283.1:p.Ser459=
XR_933266.1:n.1749C>A
XR_933267.1:n.1749C>A
XM_011522981.3:c.1377C>A	XP_011521283.1:p.Ser459=
XM_024450224.1:c.822C>A	XP_024305992.1:p.Ser274=
XR_001751889.1:n.1686C>A
XR_933266.2:n.1749C>A
NM_015386.3:c.1803C>A MANE Select	NP_056201.2:p.Ser601=
NM_001195139.2:c.1728C>A	NP_001182068.2:p.Ser576=
NM_001365426.1:c.1377C>A	NP_001352355.1:p.Ser459=
NR_158212.1:n.1762C>A