Canonical Allele Identifier: CA396580785

Gene: COG4

Linked Data

• MyVariant Identifiers: chr16:g.70517852G>C (hg19) ; chr16:g.70483949G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70483949G>C , CM000678.2:g.70483949G>C	GRCh38
NC_000016.9:g.70517852G>C , CM000678.1:g.70517852G>C	GRCh37
NC_000016.8:g.69075353G>C	NCBI36
NG_027529.1:g.44606C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534772.2:c.*1807C>G	ENSP00000461912.2:n.*1807C>G
ENST00000703106.1:c.1776C>G	ENSP00000515173.1:n.1776C>G
ENST00000703107.1:c.*1660C>G	ENSP00000515174.1:n.*1660C>G
ENST00000703108.1:c.*179C>G	ENSP00000515175.1:n.*179C>G
ENST00000703109.1:c.1764C>G	ENSP00000515176.1:p.Phe588Leu
ENST00000703110.1:c.*1233C>G	ENSP00000515177.1:n.*1233C>G
ENST00000703111.1:n.1738C>G
ENST00000703112.1:n.2504C>G
ENST00000703113.1:c.*1144C>G	ENSP00000515178.1:n.*1144C>G
ENST00000703114.1:c.*380C>G	ENSP00000515179.1:n.*380C>G
ENST00000703115.1:c.844C>G	ENSP00000515180.1:n.844C>G
ENST00000323786.10:c.1731C>G MANE Select	ENSP00000315775.5:p.Phe577Leu
ENST00000564415.6:c.*1511C>G	ENSP00000456653.2:n.*1511C>G
ENST00000674443.1:c.1656C>G	ENSP00000501405.1:p.Phe552Leu
ENST00000323786.9:c.1731C>G	ENSP00000315775.5:p.Phe577Leu
ENST00000393612.8:c.1668C>G	ENSP00000377236.5:p.Phe556Leu
ENST00000482252.5:c.1878C>G	ENSP00000432802.1:n.1878C>G
ENST00000526700.5:n.907C>G
ENST00000530314.5:n.2410C>G
ENST00000564315.1:n.191C>G
ENST00000564415.5:c.*1511C>G	ENSP00000456653.1:n.*1511C>G
NM_001195139.1:c.1668C>G	NP_001182068.1:p.Phe556Leu
NM_015386.2:c.1731C>G	NP_056201.2:p.Phe577Leu
XM_011522981.1:c.1305C>G	XP_011521283.1:p.Phe435Leu
XR_933266.1:n.1677C>G
XR_933267.1:n.1677C>G
XM_011522981.3:c.1305C>G	XP_011521283.1:p.Phe435Leu
XM_024450224.1:c.750C>G	XP_024305992.1:p.Phe250Leu
XR_001751889.1:n.1614C>G
XR_933266.2:n.1677C>G
NM_015386.3:c.1731C>G MANE Select	NP_056201.2:p.Phe577Leu
NM_001195139.2:c.1656C>G	NP_001182068.2:p.Phe552Leu
NM_001365426.1:c.1305C>G	NP_001352355.1:p.Phe435Leu
NR_158212.1:n.1690C>G