Canonical Allele Identifier: CA1141600069
Gene: COG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230690130C= , CM000663.2:g.230690130C= GRCh38
NC_000001.10:g.230825876C= , CM000663.1:g.230825876C= GRCh37
NC_000001.9:g.228892499C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366669.9:c.1911C= MANE Select ENSP00000355629.4:p.Gly637=
ENST00000366668.7:c.1908C= ENSP00000355628.3:p.Gly636=
ENST00000366669.8:c.1911C= ENSP00000355629.4:p.Gly637=
ENST00000468893.6:c.*1769C= ENSP00000476305.1:n.*1769C=
ENST00000478710.1:n.170C=
ENST00000490900.1:n.690C=
ENST00000534989.1:c.1734C= ENSP00000440349.1:p.Gly578=
NM_001145036.1:c.1908C= NP_001138508.1:p.Gly636=
NM_007357.2:c.1911C= NP_031383.1:p.Gly637=
NM_007357.3:c.1911C= MANE Select NP_031383.1:p.Gly637=
NM_001145036.2:c.1908C= NP_001138508.1:p.Gly636=