Canonical Allele Identifier: CA345198947
Gene: COG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230690120G>T , CM000663.2:g.230690120G>T GRCh38
NC_000001.10:g.230825866G>T , CM000663.1:g.230825866G>T GRCh37
NC_000001.9:g.228892489G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366669.9:c.1901G>T MANE Select ENSP00000355629.4:p.Trp634Leu
ENST00000366668.7:c.1898G>T ENSP00000355628.3:p.Trp633Leu
ENST00000366669.8:c.1901G>T ENSP00000355629.4:p.Trp634Leu
ENST00000468893.6:c.*1759G>T ENSP00000476305.1:n.*1759G>T
ENST00000478710.1:n.160G>T
ENST00000490900.1:n.680G>T
ENST00000534989.1:c.1724G>T ENSP00000440349.1:p.Trp575Leu
NM_001145036.1:c.1898G>T NP_001138508.1:p.Trp633Leu
NM_007357.2:c.1901G>T NP_031383.1:p.Trp634Leu
NM_007357.3:c.1901G>T MANE Select NP_031383.1:p.Trp634Leu
NM_001145036.2:c.1898G>T NP_001138508.1:p.Trp633Leu