Canonical Allele Identifier: CA400880908
Gene: COG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73193376G>T , CM000679.2:g.73193376G>T GRCh38
NC_000017.10:g.71189515G>T , CM000679.1:g.71189515G>T GRCh37
NC_000017.9:g.68701110G>T NCBI36
NG_008971.1:g.5343G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000299886.9:c.307G>T MANE Select ENSP00000299886.4:p.Ala103Ser
ENST00000299886.8:c.307G>T ENSP00000299886.4:p.Ala103Ser
ENST00000438720.7:c.305G>T
ENST00000582587.2:c.284G>T
ENST00000618996.4:c.307G>T ENSP00000479450.1:p.Ala103Ser
NM_018714.2:c.307G>T NP_061184.1:p.Ala103Ser
NM_018714.3:c.307G>T MANE Select NP_061184.1:p.Ala103Ser