Canonical Allele Identifier: CA423878744

Gene: COG2

Linked Data

• dbSNP Id: rs2102775670
• MyVariant Identifiers: chr1:g.230825804G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230690058G>A , CM000663.2:g.230690058G>A	GRCh38
NC_000001.10:g.230825804G>A , CM000663.1:g.230825804G>A	GRCh37
NC_000001.9:g.228892427G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366669.9:c.1839G>A MANE Select	ENSP00000355629.4:p.Lys613=
ENST00000366668.7:c.1836G>A	ENSP00000355628.3:p.Lys612=
ENST00000366669.8:c.1839G>A	ENSP00000355629.4:p.Lys613=
ENST00000468893.6:c.*1697G>A	ENSP00000476305.1:n.*1697G>A
ENST00000478710.1:n.98G>A
ENST00000490900.1:n.618G>A
ENST00000534989.1:c.1662G>A	ENSP00000440349.1:p.Lys554=
NM_001145036.1:c.1836G>A	NP_001138508.1:p.Lys612=
NM_007357.2:c.1839G>A	NP_031383.1:p.Lys613=
NM_007357.3:c.1839G>A MANE Select	NP_031383.1:p.Lys613=
NM_001145036.2:c.1836G>A	NP_001138508.1:p.Lys612=