Canonical Allele Identifier: CA423879401

Gene: COG2

Linked Data

• MyVariant Identifiers: chr1:g.230825894T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230690148T>C , CM000663.2:g.230690148T>C	GRCh38
NC_000001.10:g.230825894T>C , CM000663.1:g.230825894T>C	GRCh37
NC_000001.9:g.228892517T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366669.9:c.1929T>C MANE Select	ENSP00000355629.4:p.Thr643=
ENST00000366668.7:c.1926T>C	ENSP00000355628.3:p.Thr642=
ENST00000366669.8:c.1929T>C	ENSP00000355629.4:p.Thr643=
ENST00000468893.6:c.*1787T>C	ENSP00000476305.1:n.*1787T>C
ENST00000478710.1:n.188T>C
ENST00000490900.1:n.708T>C
ENST00000534989.1:c.1752T>C	ENSP00000440349.1:p.Thr584=
NM_001145036.1:c.1926T>C	NP_001138508.1:p.Thr642=
NM_007357.2:c.1929T>C	NP_031383.1:p.Thr643=
NM_007357.3:c.1929T>C MANE Select	NP_031383.1:p.Thr643=
NM_001145036.2:c.1926T>C	NP_001138508.1:p.Thr642=