Canonical Allele Identifier: CA2086088060

Gene: COG6

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.39699396A= , CM000675.2:g.39699396A=	GRCh38
NC_000013.10:g.40273533A= , CM000675.1:g.40273533A=	GRCh37
NC_000013.9:g.39171533A=	NCBI36
NG_028352.1:g.48770A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000455146.8:c.1167-105A= MANE Select	ENSP00000397441.2:n.1167-105A=
ENST00000356576.8:c.*1004-105A=	ENSP00000348983.4:n.*1004-105A=
ENST00000416691.5:c.1167-105A=	ENSP00000403733.1:n.1167-105A=
ENST00000455146.7:c.1167-105A=	ENSP00000397441.2:n.1167-105A=
NM_001145079.1:c.1167-105A=	NP_001138551.1:n.1167-105A=
NM_020751.2:c.1167-105A=	NP_065802.1:n.1167-105A=
NR_026745.1:n.1332-105A=
XM_011535168.1:c.1167-105A=	XP_011533470.1:n.1167-105A=
XM_011535169.1:c.1011-105A=	XP_011533471.1:n.1011-105A=
XM_011535170.1:c.1011-105A=	XP_011533472.1:n.1011-105A=
NM_020751.3:c.1167-105A= MANE Select	NP_065802.1:n.1167-105A=
NM_001145079.2:c.1167-105A=	NP_001138551.1:n.1167-105A=