Canonical Allele Identifier: CA2274431862
Gene: COG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73196362C= , CM000679.2:g.73196362C= GRCh38
NC_000017.10:g.71192501C= , CM000679.1:g.71192501C= GRCh37
NC_000017.9:g.68704096C= NCBI36
NG_008971.1:g.8329C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299886.9:c.316-145C= MANE Select ENSP00000299886.4:n.316-145C=
ENST00000299886.8:c.316-145C= ENSP00000299886.4:n.316-145C=
ENST00000438720.7:c.314-145C=
ENST00000582587.2:c.293-125C=
ENST00000618996.4:c.316-145C= ENSP00000479450.1:n.316-145C=
NM_018714.2:c.316-145C= NP_061184.1:n.316-145C=
NM_018714.3:c.316-145C= MANE Select NP_061184.1:n.316-145C=