Canonical Allele Identifier: CA396580632

Gene: COG4

Linked Data

• MyVariant Identifiers: chr16:g.70517782A>T (hg19) ; chr16:g.70483879A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70483879A>T , CM000678.2:g.70483879A>T	GRCh38
NC_000016.9:g.70517782A>T , CM000678.1:g.70517782A>T	GRCh37
NC_000016.8:g.69075283A>T	NCBI36
NG_027529.1:g.44676T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000534772.2:c.*1877T>A	ENSP00000461912.2:n.*1877T>A
ENST00000703106.1:c.1846T>A	ENSP00000515173.1:n.1846T>A
ENST00000703107.1:c.*1730T>A	ENSP00000515174.1:n.*1730T>A
ENST00000703108.1:c.*249T>A	ENSP00000515175.1:n.*249T>A
ENST00000703109.1:c.1834T>A	ENSP00000515176.1:p.Ser612Thr
ENST00000703110.1:c.*1303T>A	ENSP00000515177.1:n.*1303T>A
ENST00000703111.1:n.1808T>A
ENST00000703112.1:n.2574T>A
ENST00000703113.1:c.*1214T>A	ENSP00000515178.1:n.*1214T>A
ENST00000703114.1:c.*450T>A	ENSP00000515179.1:n.*450T>A
ENST00000703115.1:c.914T>A	ENSP00000515180.1:n.914T>A
ENST00000323786.10:c.1801T>A MANE Select	ENSP00000315775.5:p.Ser601Thr
ENST00000564415.6:c.*1581T>A	ENSP00000456653.2:n.*1581T>A
ENST00000674443.1:c.1726T>A	ENSP00000501405.1:p.Ser576Thr
ENST00000323786.9:c.1801T>A	ENSP00000315775.5:p.Ser601Thr
ENST00000393612.8:c.1738T>A	ENSP00000377236.5:p.Ser580Thr
ENST00000482252.5:c.1948T>A	ENSP00000432802.1:n.1948T>A
ENST00000526700.5:n.977T>A
ENST00000530314.5:n.2480T>A
ENST00000564315.1:n.261T>A
ENST00000564415.5:c.*1581T>A	ENSP00000456653.1:n.*1581T>A
NM_001195139.1:c.1738T>A	NP_001182068.1:p.Ser580Thr
NM_015386.2:c.1801T>A	NP_056201.2:p.Ser601Thr
XM_011522981.1:c.1375T>A	XP_011521283.1:p.Ser459Thr
XR_933266.1:n.1747T>A
XR_933267.1:n.1747T>A
XM_011522981.3:c.1375T>A	XP_011521283.1:p.Ser459Thr
XM_024450224.1:c.820T>A	XP_024305992.1:p.Ser274Thr
XR_001751889.1:n.1684T>A
XR_933266.2:n.1747T>A
NM_015386.3:c.1801T>A MANE Select	NP_056201.2:p.Ser601Thr
NM_001195139.2:c.1726T>A	NP_001182068.2:p.Ser576Thr
NM_001365426.1:c.1375T>A	NP_001352355.1:p.Ser459Thr
NR_158212.1:n.1760T>A