Canonical Allele Identifier: CA2274431818
Gene: COG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73196251T= , CM000679.2:g.73196251T= GRCh38
NC_000017.10:g.71192390T= , CM000679.1:g.71192390T= GRCh37
NC_000017.9:g.68703985T= NCBI36
NG_008971.1:g.8218T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299886.9:c.316-256T= MANE Select ENSP00000299886.4:n.316-256T=
ENST00000299886.8:c.316-256T= ENSP00000299886.4:n.316-256T=
ENST00000438720.7:c.314-256T=
ENST00000582587.2:c.293-236T=
ENST00000618996.4:c.316-256T= ENSP00000479450.1:n.316-256T=
NM_018714.2:c.316-256T= NP_061184.1:n.316-256T=
NM_018714.3:c.316-256T= MANE Select NP_061184.1:n.316-256T=