Canonical Allele Identifier: CA423879199

Gene: COG2

Linked Data

• MyVariant Identifiers: chr1:g.230825864G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230690118G>A , CM000663.2:g.230690118G>A	GRCh38
NC_000001.10:g.230825864G>A , CM000663.1:g.230825864G>A	GRCh37
NC_000001.9:g.228892487G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366669.9:c.1899G>A MANE Select	ENSP00000355629.4:p.Gln633=
ENST00000366668.7:c.1896G>A	ENSP00000355628.3:p.Gln632=
ENST00000366669.8:c.1899G>A	ENSP00000355629.4:p.Gln633=
ENST00000468893.6:c.*1757G>A	ENSP00000476305.1:n.*1757G>A
ENST00000478710.1:n.158G>A
ENST00000490900.1:n.678G>A
ENST00000534989.1:c.1722G>A	ENSP00000440349.1:p.Gln574=
NM_001145036.1:c.1896G>A	NP_001138508.1:p.Gln632=
NM_007357.2:c.1899G>A	NP_031383.1:p.Gln633=
NM_007357.3:c.1899G>A MANE Select	NP_031383.1:p.Gln633=
NM_001145036.2:c.1896G>A	NP_001138508.1:p.Gln632=