Canonical Allele Identifier: CA2274430363
Gene: COG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73193279C= , CM000679.2:g.73193279C= GRCh38
NC_000017.10:g.71189418C= , CM000679.1:g.71189418C= GRCh37
NC_000017.9:g.68701013C= NCBI36
NG_008971.1:g.5246C=

Transcript Alleles

HGVS Amino-acid change
ENST00000299886.9:c.210C= MANE Select ENSP00000299886.4:p.Arg70=
ENST00000299886.8:c.210C= ENSP00000299886.4:p.Arg70=
ENST00000438720.7:c.208C=
ENST00000582587.2:c.187C=
ENST00000618996.4:c.210C= ENSP00000479450.1:p.Arg70=
NM_018714.2:c.210C= NP_061184.1:p.Arg70=
NM_018714.3:c.210C= MANE Select NP_061184.1:p.Arg70=