Canonical Allele Identifier: CA2086088084
Gene: COG6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.39699477A= , CM000675.2:g.39699477A= GRCh38
NC_000013.10:g.40273614A= , CM000675.1:g.40273614A= GRCh37
NC_000013.9:g.39171614A= NCBI36
NG_028352.1:g.48851A=

Transcript Alleles

HGVS Amino-acid Change
NM_020751.3:c.1167-24A= MANE Select NP_065802.1:n.1167-24A=
ENST00000455146.8:c.1167-24A= MANE Select ENSP00000397441.2:n.1167-24A=
NM_001145079.1:c.1167-24A= NP_001138551.1:n.1167-24A=
NM_001145079.2:c.1167-24A= NP_001138551.1:n.1167-24A=
NM_020751.2:c.1167-24A= NP_065802.1:n.1167-24A=
NR_026745.1:n.1332-24A=
ENST00000356576.8:c.*1004-24A= ENSP00000348983.4:n.*1004-24A=
ENST00000416691.5:c.1167-24A= ENSP00000403733.1:n.1167-24A=
ENST00000455146.7:c.1167-24A= ENSP00000397441.2:n.1167-24A=
XM_011535168.1:c.1167-24A= XP_011533470.1:n.1167-24A=
XM_011535169.1:c.1011-24A= XP_011533471.1:n.1011-24A=
XM_011535170.1:c.1011-24A= XP_011533472.1:n.1011-24A=