Canonical Allele Identifier: CA2274430359
Gene: COG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73193273G= , CM000679.2:g.73193273G= GRCh38
NC_000017.10:g.71189412G= , CM000679.1:g.71189412G= GRCh37
NC_000017.9:g.68701007G= NCBI36
NG_008971.1:g.5240G=

Transcript Alleles

HGVS Amino-acid change
ENST00000299886.9:c.204G= MANE Select ENSP00000299886.4:p.Gln68=
ENST00000299886.8:c.204G= ENSP00000299886.4:p.Gln68=
ENST00000438720.7:c.202G=
ENST00000582587.2:c.181G=
ENST00000618996.4:c.204G= ENSP00000479450.1:p.Gln68=
NM_018714.2:c.204G= NP_061184.1:p.Gln68=
NM_018714.3:c.204G= MANE Select NP_061184.1:p.Gln68=