Canonical Allele Identifier: CA2274431844
Gene: COG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73196331C= , CM000679.2:g.73196331C= GRCh38
NC_000017.10:g.71192470C= , CM000679.1:g.71192470C= GRCh37
NC_000017.9:g.68704065C= NCBI36
NG_008971.1:g.8298C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299886.9:c.316-176C= MANE Select ENSP00000299886.4:n.316-176C=
ENST00000299886.8:c.316-176C= ENSP00000299886.4:n.316-176C=
ENST00000438720.7:c.314-176C=
ENST00000582587.2:c.293-156C=
ENST00000618996.4:c.316-176C= ENSP00000479450.1:n.316-176C=
NM_018714.2:c.316-176C= NP_061184.1:n.316-176C=
NM_018714.3:c.316-176C= MANE Select NP_061184.1:n.316-176C=
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