Canonical Allele Identifier: CA400879795
Gene: COG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73193272A>C , CM000679.2:g.73193272A>C GRCh38
NC_000017.10:g.71189411A>C , CM000679.1:g.71189411A>C GRCh37
NC_000017.9:g.68701006A>C NCBI36
NG_008971.1:g.5239A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000299886.9:c.203A>C MANE Select ENSP00000299886.4:p.Gln68Pro
ENST00000299886.8:c.203A>C ENSP00000299886.4:p.Gln68Pro
ENST00000438720.7:c.201A>C
ENST00000582587.2:c.180A>C
ENST00000618996.4:c.203A>C ENSP00000479450.1:p.Gln68Pro
NM_018714.2:c.203A>C NP_061184.1:p.Gln68Pro
NM_018714.3:c.203A>C MANE Select NP_061184.1:p.Gln68Pro