Canonical Allele Identifier: CA423878794

Gene: COG2

Linked Data

• MyVariant Identifiers: chr1:g.230825813C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230690067C>T , CM000663.2:g.230690067C>T	GRCh38
NC_000001.10:g.230825813C>T , CM000663.1:g.230825813C>T	GRCh37
NC_000001.9:g.228892436C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366669.9:c.1848C>T MANE Select	ENSP00000355629.4:p.Phe616=
ENST00000366668.7:c.1845C>T	ENSP00000355628.3:p.Phe615=
ENST00000366669.8:c.1848C>T	ENSP00000355629.4:p.Phe616=
ENST00000468893.6:c.*1706C>T	ENSP00000476305.1:n.*1706C>T
ENST00000478710.1:n.107C>T
ENST00000490900.1:n.627C>T
ENST00000534989.1:c.1671C>T	ENSP00000440349.1:p.Phe557=
NM_001145036.1:c.1845C>T	NP_001138508.1:p.Phe615=
NM_007357.2:c.1848C>T	NP_031383.1:p.Phe616=
NM_007357.3:c.1848C>T MANE Select	NP_031383.1:p.Phe616=
NM_001145036.2:c.1845C>T	NP_001138508.1:p.Phe615=