Canonical Allele Identifier: CA2086088063
Gene: COG6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.39699404T= , CM000675.2:g.39699404T= GRCh38
NC_000013.10:g.40273541T= , CM000675.1:g.40273541T= GRCh37
NC_000013.9:g.39171541T= NCBI36
NG_028352.1:g.48778T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000455146.8:c.1167-97T= MANE Select ENSP00000397441.2:n.1167-97T=
ENST00000356576.8:c.*1004-97T= ENSP00000348983.4:n.*1004-97T=
ENST00000416691.5:c.1167-97T= ENSP00000403733.1:n.1167-97T=
ENST00000455146.7:c.1167-97T= ENSP00000397441.2:n.1167-97T=
NM_001145079.1:c.1167-97T= NP_001138551.1:n.1167-97T=
NM_020751.2:c.1167-97T= NP_065802.1:n.1167-97T=
NR_026745.1:n.1332-97T=
XM_011535168.1:c.1167-97T= XP_011533470.1:n.1167-97T=
XM_011535169.1:c.1011-97T= XP_011533471.1:n.1011-97T=
XM_011535170.1:c.1011-97T= XP_011533472.1:n.1011-97T=
NM_020751.3:c.1167-97T= MANE Select NP_065802.1:n.1167-97T=
NM_001145079.2:c.1167-97T= NP_001138551.1:n.1167-97T=