Canonical Allele Identifier: CA2622752761

Gene: COG6

Linked Data

• gnomAD v4: 13-39699393-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.39699393C>A , CM000675.2:g.39699393C>A	GRCh38
NC_000013.10:g.40273530C>A , CM000675.1:g.40273530C>A	GRCh37
NC_000013.9:g.39171530C>A	NCBI36
NG_028352.1:g.48767C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455146.8:c.1167-108C>A MANE Select	ENSP00000397441.2:n.1167-108C>A
ENST00000356576.8:c.*1004-108C>A	ENSP00000348983.4:n.*1004-108C>A
ENST00000416691.5:c.1167-108C>A	ENSP00000403733.1:n.1167-108C>A
ENST00000455146.7:c.1167-108C>A	ENSP00000397441.2:n.1167-108C>A
NM_001145079.1:c.1167-108C>A	NP_001138551.1:n.1167-108C>A
NM_020751.2:c.1167-108C>A	NP_065802.1:n.1167-108C>A
NR_026745.1:n.1332-108C>A
XM_011535168.1:c.1167-108C>A	XP_011533470.1:n.1167-108C>A
XM_011535169.1:c.1011-108C>A	XP_011533471.1:n.1011-108C>A
XM_011535170.1:c.1011-108C>A	XP_011533472.1:n.1011-108C>A
NM_020751.3:c.1167-108C>A MANE Select	NP_065802.1:n.1167-108C>A
NM_001145079.2:c.1167-108C>A	NP_001138551.1:n.1167-108C>A