Canonical Allele Identifier: CA400883213
Gene: COG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73196600G>T , CM000679.2:g.73196600G>T GRCh38
NC_000017.10:g.71192739G>T , CM000679.1:g.71192739G>T GRCh37
NC_000017.9:g.68704334G>T NCBI36
NG_008971.1:g.8567G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299886.9:c.409G>T MANE Select ENSP00000299886.4:p.Ala137Ser
ENST00000299886.8:c.409G>T ENSP00000299886.4:p.Ala137Ser
ENST00000438720.7:c.407G>T
ENST00000582587.2:c.406G>T
ENST00000618996.4:c.409G>T ENSP00000479450.1:p.Ala137Ser
NM_018714.2:c.409G>T NP_061184.1:p.Ala137Ser
NM_018714.3:c.409G>T MANE Select NP_061184.1:p.Ala137Ser