Canonical Allele Identifier: CA400880999
Gene: COG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73193382C>G , CM000679.2:g.73193382C>G GRCh38
NC_000017.10:g.71189521C>G , CM000679.1:g.71189521C>G GRCh37
NC_000017.9:g.68701116C>G NCBI36
NG_008971.1:g.5349C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000299886.9:c.313C>G MANE Select ENSP00000299886.4:p.Gln105Glu
ENST00000299886.8:c.313C>G ENSP00000299886.4:p.Gln105Glu
ENST00000438720.7:c.311C>G
ENST00000582587.2:c.290C>G
ENST00000618996.4:c.313C>G ENSP00000479450.1:p.Gln105Glu
NM_018714.2:c.313C>G NP_061184.1:p.Gln105Glu
NM_018714.3:c.313C>G MANE Select NP_061184.1:p.Gln105Glu