Canonical Allele Identifier: CA396580643

Gene: COG4

Linked Data

• COSMIC: COSM6454023
• MyVariant Identifiers: chr16:g.70517790G>A (hg19) ; chr16:g.70483887G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70483887G>A , CM000678.2:g.70483887G>A	GRCh38
NC_000016.9:g.70517790G>A , CM000678.1:g.70517790G>A	GRCh37
NC_000016.8:g.69075291G>A	NCBI36
NG_027529.1:g.44668C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000534772.2:c.*1869C>T	ENSP00000461912.2:n.*1869C>T
ENST00000703106.1:c.1838C>T	ENSP00000515173.1:n.1838C>T
ENST00000703107.1:c.*1722C>T	ENSP00000515174.1:n.*1722C>T
ENST00000703108.1:c.*241C>T	ENSP00000515175.1:n.*241C>T
ENST00000703109.1:c.1826C>T	ENSP00000515176.1:p.Ala609Val
ENST00000703110.1:c.*1295C>T	ENSP00000515177.1:n.*1295C>T
ENST00000703111.1:n.1800C>T
ENST00000703112.1:n.2566C>T
ENST00000703113.1:c.*1206C>T	ENSP00000515178.1:n.*1206C>T
ENST00000703114.1:c.*442C>T	ENSP00000515179.1:n.*442C>T
ENST00000703115.1:c.906C>T	ENSP00000515180.1:n.906C>T
ENST00000323786.10:c.1793C>T MANE Select	ENSP00000315775.5:p.Ala598Val
ENST00000564415.6:c.*1573C>T	ENSP00000456653.2:n.*1573C>T
ENST00000674443.1:c.1718C>T	ENSP00000501405.1:p.Ala573Val
ENST00000323786.9:c.1793C>T	ENSP00000315775.5:p.Ala598Val
ENST00000393612.8:c.1730C>T	ENSP00000377236.5:p.Ala577Val
ENST00000482252.5:c.1940C>T	ENSP00000432802.1:n.1940C>T
ENST00000526700.5:n.969C>T
ENST00000530314.5:n.2472C>T
ENST00000564315.1:n.253C>T
ENST00000564415.5:c.*1573C>T	ENSP00000456653.1:n.*1573C>T
NM_001195139.1:c.1730C>T	NP_001182068.1:p.Ala577Val
NM_015386.2:c.1793C>T	NP_056201.2:p.Ala598Val
XM_011522981.1:c.1367C>T	XP_011521283.1:p.Ala456Val
XR_933266.1:n.1739C>T
XR_933267.1:n.1739C>T
XM_011522981.3:c.1367C>T	XP_011521283.1:p.Ala456Val
XM_024450224.1:c.812C>T	XP_024305992.1:p.Ala271Val
XR_001751889.1:n.1676C>T
XR_933266.2:n.1739C>T
NM_015386.3:c.1793C>T MANE Select	NP_056201.2:p.Ala598Val
NM_001195139.2:c.1718C>T	NP_001182068.2:p.Ala573Val
NM_001365426.1:c.1367C>T	NP_001352355.1:p.Ala456Val
NR_158212.1:n.1752C>T