Canonical Allele Identifier: CA2230785022
Gene: COG4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.70481439G= , CM000678.2:g.70481439G= GRCh38
NC_000016.9:g.70515342G= , CM000678.1:g.70515342G= GRCh37
NC_000016.8:g.69072843G= NCBI36
NG_027529.1:g.47116C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000534772.2:c.*2231C= ENSP00000461912.2:n.*2231C=
ENST00000703106.1:c.2200C= ENSP00000515173.1:n.2200C=
ENST00000703107.1:c.*2084C= ENSP00000515174.1:n.*2084C=
ENST00000703108.1:c.*603C= ENSP00000515175.1:n.*603C=
ENST00000703109.1:c.2188C= ENSP00000515176.1:p.Leu730=
ENST00000703110.1:c.*1657C= ENSP00000515177.1:n.*1657C=
ENST00000703111.1:n.2438C=
ENST00000703112.1:n.3099C=
ENST00000703113.1:c.*1568C= ENSP00000515178.1:n.*1568C=
ENST00000703114.1:c.*804C= ENSP00000515179.1:n.*804C=
ENST00000703115.1:c.1268C= ENSP00000515180.1:n.1268C=
ENST00000323786.10:c.2155C= MANE Select ENSP00000315775.5:p.Leu719=
ENST00000564415.6:c.*1935C= ENSP00000456653.2:n.*1935C=
ENST00000674443.1:c.2080C= ENSP00000501405.1:p.Leu694=
ENST00000323786.9:c.2155C= ENSP00000315775.5:p.Leu719=
ENST00000393612.8:c.2092C= ENSP00000377236.5:p.Leu698=
ENST00000482252.5:c.2302C= ENSP00000432802.1:n.2302C=
ENST00000526700.5:n.1331C=
ENST00000530314.5:n.2834C=
ENST00000564415.5:c.*1935C= ENSP00000456653.1:n.*1935C=
ENST00000565715.1:c.217C= ENSP00000455693.1:p.Leu73=
NM_001195139.1:c.2092C= NP_001182068.1:p.Leu698=
NM_015386.2:c.2155C= NP_056201.2:p.Leu719=
XM_011522981.1:c.1729C= XP_011521283.1:p.Leu577=
XM_011522981.3:c.1729C= XP_011521283.1:p.Leu577=
XM_024450224.1:c.1174C= XP_024305992.1:p.Leu392=
XR_933266.2:n.2101C=
NM_015386.3:c.2155C= MANE Select NP_056201.2:p.Leu719=
NM_001195139.2:c.2080C= NP_001182068.2:p.Leu694=
NM_001365426.1:c.1729C= NP_001352355.1:p.Leu577=
NR_158212.1:n.2114C=