Canonical Allele Identifier: CA396578055
Gene: COG4 HGNC NCBI

Linked Data

dbSNP Id: rs769274001

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.70481399G>T , CM000678.2:g.70481399G>T GRCh38
NC_000016.9:g.70515302G>T , CM000678.1:g.70515302G>T GRCh37
NC_000016.8:g.69072803G>T NCBI36
NG_027529.1:g.47156C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000534772.2:c.*2271C>A ENSP00000461912.2:n.*2271C>A
ENST00000703106.1:c.2240C>A ENSP00000515173.1:n.2240C>A
ENST00000703107.1:c.*2124C>A ENSP00000515174.1:n.*2124C>A
ENST00000703108.1:c.*643C>A ENSP00000515175.1:n.*643C>A
ENST00000703109.1:c.2228C>A ENSP00000515176.1:p.Ala743Asp
ENST00000703110.1:c.*1697C>A ENSP00000515177.1:n.*1697C>A
ENST00000703111.1:n.2478C>A
ENST00000703112.1:n.3139C>A
ENST00000703113.1:c.*1608C>A ENSP00000515178.1:n.*1608C>A
ENST00000703114.1:c.*844C>A ENSP00000515179.1:n.*844C>A
ENST00000703115.1:c.1308C>A ENSP00000515180.1:n.1308C>A
ENST00000323786.10:c.2195C>A MANE Select ENSP00000315775.5:p.Ala732Asp
ENST00000564415.6:c.*1975C>A ENSP00000456653.2:n.*1975C>A
ENST00000674443.1:c.2120C>A ENSP00000501405.1:p.Ala707Asp
ENST00000323786.9:c.2195C>A ENSP00000315775.5:p.Ala732Asp
ENST00000393612.8:c.2132C>A ENSP00000377236.5:p.Ala711Asp
ENST00000482252.5:c.2342C>A ENSP00000432802.1:n.2342C>A
ENST00000526700.5:n.1371C>A
ENST00000530314.5:n.2874C>A
ENST00000564415.5:c.*1975C>A ENSP00000456653.1:n.*1975C>A
ENST00000565715.1:c.257C>A ENSP00000455693.1:p.Ala86Asp
NM_001195139.1:c.2132C>A NP_001182068.1:p.Ala711Asp
NM_015386.2:c.2195C>A NP_056201.2:p.Ala732Asp
XM_011522981.1:c.1769C>A XP_011521283.1:p.Ala590Asp
XM_011522981.3:c.1769C>A XP_011521283.1:p.Ala590Asp
XM_024450224.1:c.1214C>A XP_024305992.1:p.Ala405Asp
XR_933266.2:n.2141C>A
NM_015386.3:c.2195C>A MANE Select NP_056201.2:p.Ala732Asp
NM_001195139.2:c.2120C>A NP_001182068.2:p.Ala707Asp
NM_001365426.1:c.1769C>A NP_001352355.1:p.Ala590Asp
NR_158212.1:n.2154C>A