Canonical Allele Identifier: CA396580769

Gene: COG4

Linked Data

• MyVariant Identifiers: chr16:g.70517845C>T (hg19) ; chr16:g.70483942C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70483942C>T , CM000678.2:g.70483942C>T	GRCh38
NC_000016.9:g.70517845C>T , CM000678.1:g.70517845C>T	GRCh37
NC_000016.8:g.69075346C>T	NCBI36
NG_027529.1:g.44613G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534772.2:c.*1814G>A	ENSP00000461912.2:n.*1814G>A
ENST00000703106.1:c.1783G>A	ENSP00000515173.1:n.1783G>A
ENST00000703107.1:c.*1667G>A	ENSP00000515174.1:n.*1667G>A
ENST00000703108.1:c.*186G>A	ENSP00000515175.1:n.*186G>A
ENST00000703109.1:c.1771G>A	ENSP00000515176.1:p.Gly591Ser
ENST00000703110.1:c.*1240G>A	ENSP00000515177.1:n.*1240G>A
ENST00000703111.1:n.1745G>A
ENST00000703112.1:n.2511G>A
ENST00000703113.1:c.*1151G>A	ENSP00000515178.1:n.*1151G>A
ENST00000703114.1:c.*387G>A	ENSP00000515179.1:n.*387G>A
ENST00000703115.1:c.851G>A	ENSP00000515180.1:n.851G>A
ENST00000323786.10:c.1738G>A MANE Select	ENSP00000315775.5:p.Gly580Ser
ENST00000564415.6:c.*1518G>A	ENSP00000456653.2:n.*1518G>A
ENST00000674443.1:c.1663G>A	ENSP00000501405.1:p.Gly555Ser
ENST00000323786.9:c.1738G>A	ENSP00000315775.5:p.Gly580Ser
ENST00000393612.8:c.1675G>A	ENSP00000377236.5:p.Gly559Ser
ENST00000482252.5:c.1885G>A	ENSP00000432802.1:n.1885G>A
ENST00000526700.5:n.914G>A
ENST00000530314.5:n.2417G>A
ENST00000564315.1:n.198G>A
ENST00000564415.5:c.*1518G>A	ENSP00000456653.1:n.*1518G>A
NM_001195139.1:c.1675G>A	NP_001182068.1:p.Gly559Ser
NM_015386.2:c.1738G>A	NP_056201.2:p.Gly580Ser
XM_011522981.1:c.1312G>A	XP_011521283.1:p.Gly438Ser
XR_933266.1:n.1684G>A
XR_933267.1:n.1684G>A
XM_011522981.3:c.1312G>A	XP_011521283.1:p.Gly438Ser
XM_024450224.1:c.757G>A	XP_024305992.1:p.Gly253Ser
XR_001751889.1:n.1621G>A
XR_933266.2:n.1684G>A
NM_015386.3:c.1738G>A MANE Select	NP_056201.2:p.Gly580Ser
NM_001195139.2:c.1663G>A	NP_001182068.2:p.Gly555Ser
NM_001365426.1:c.1312G>A	NP_001352355.1:p.Gly438Ser
NR_158212.1:n.1697G>A