Canonical Allele Identifier: CA2230785025
Gene: COG4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.70481447A= , CM000678.2:g.70481447A= GRCh38
NC_000016.9:g.70515350A= , CM000678.1:g.70515350A= GRCh37
NC_000016.8:g.69072851A= NCBI36
NG_027529.1:g.47108T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000534772.2:c.*2223T= ENSP00000461912.2:n.*2223T=
ENST00000703106.1:c.2192T= ENSP00000515173.1:n.2192T=
ENST00000703107.1:c.*2076T= ENSP00000515174.1:n.*2076T=
ENST00000703108.1:c.*595T= ENSP00000515175.1:n.*595T=
ENST00000703109.1:c.2180T= ENSP00000515176.1:p.Ile727=
ENST00000703110.1:c.*1649T= ENSP00000515177.1:n.*1649T=
ENST00000703111.1:n.2430T=
ENST00000703112.1:n.3091T=
ENST00000703113.1:c.*1560T= ENSP00000515178.1:n.*1560T=
ENST00000703114.1:c.*796T= ENSP00000515179.1:n.*796T=
ENST00000703115.1:c.1260T= ENSP00000515180.1:n.1260T=
ENST00000323786.10:c.2147T= MANE Select ENSP00000315775.5:p.Ile716=
ENST00000564415.6:c.*1927T= ENSP00000456653.2:n.*1927T=
ENST00000674443.1:c.2072T= ENSP00000501405.1:p.Ile691=
ENST00000323786.9:c.2147T= ENSP00000315775.5:p.Ile716=
ENST00000393612.8:c.2084T= ENSP00000377236.5:p.Ile695=
ENST00000482252.5:c.2294T= ENSP00000432802.1:n.2294T=
ENST00000526700.5:n.1323T=
ENST00000530314.5:n.2826T=
ENST00000564415.5:c.*1927T= ENSP00000456653.1:n.*1927T=
ENST00000565715.1:c.209T= ENSP00000455693.1:p.Ile70=
NM_001195139.1:c.2084T= NP_001182068.1:p.Ile695=
NM_015386.2:c.2147T= NP_056201.2:p.Ile716=
XM_011522981.1:c.1721T= XP_011521283.1:p.Ile574=
XM_011522981.3:c.1721T= XP_011521283.1:p.Ile574=
XM_024450224.1:c.1166T= XP_024305992.1:p.Ile389=
XR_933266.2:n.2093T=
NM_015386.3:c.2147T= MANE Select NP_056201.2:p.Ile716=
NM_001195139.2:c.2072T= NP_001182068.2:p.Ile691=
NM_001365426.1:c.1721T= NP_001352355.1:p.Ile574=
NR_158212.1:n.2106T=