Canonical Allele Identifier: CA345198961

Gene: COG2

Linked Data

• MyVariant Identifiers: chr1:g.230825873A>C (hg19) ; chr1:g.230690127A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230690127A>C , CM000663.2:g.230690127A>C	GRCh38
NC_000001.10:g.230825873A>C , CM000663.1:g.230825873A>C	GRCh37
NC_000001.9:g.228892496A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000366669.9:c.1908A>C MANE Select	ENSP00000355629.4:p.Glu636Asp
ENST00000366668.7:c.1905A>C	ENSP00000355628.3:p.Glu635Asp
ENST00000366669.8:c.1908A>C	ENSP00000355629.4:p.Glu636Asp
ENST00000468893.6:c.*1766A>C	ENSP00000476305.1:n.*1766A>C
ENST00000478710.1:n.167A>C
ENST00000490900.1:n.687A>C
ENST00000534989.1:c.1731A>C	ENSP00000440349.1:p.Glu577Asp
NM_001145036.1:c.1905A>C	NP_001138508.1:p.Glu635Asp
NM_007357.2:c.1908A>C	NP_031383.1:p.Glu636Asp
NM_007357.3:c.1908A>C MANE Select	NP_031383.1:p.Glu636Asp
NM_001145036.2:c.1905A>C	NP_001138508.1:p.Glu635Asp