Canonical Allele Identifier: CA1226660379

Gene: COG2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230690026A= , CM000663.2:g.230690026A=	GRCh38
NC_000001.10:g.230825772A= , CM000663.1:g.230825772A=	GRCh37
NC_000001.9:g.228892395A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366669.9:c.1807A= MANE Select	ENSP00000355629.4:p.Thr603=
ENST00000366668.7:c.1804A=	ENSP00000355628.3:p.Thr602=
ENST00000366669.8:c.1807A=	ENSP00000355629.4:p.Thr603=
ENST00000468893.6:c.*1665A=	ENSP00000476305.1:n.*1665A=
ENST00000478710.1:n.66A=
ENST00000490900.1:n.586A=
ENST00000534989.1:c.1630A=	ENSP00000440349.1:p.Thr544=
NM_001145036.1:c.1804A=	NP_001138508.1:p.Thr602=
NM_007357.2:c.1807A=	NP_031383.1:p.Thr603=
NM_007357.3:c.1807A= MANE Select	NP_031383.1:p.Thr603=
NM_001145036.2:c.1804A=	NP_001138508.1:p.Thr602=