Canonical Allele Identifier: CA396482816

Gene: COG8

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.69334520C>T , CM000678.2:g.69334520C>T	GRCh38
NC_000016.9:g.69368423C>T , CM000678.1:g.69368423C>T	GRCh37
NC_000016.8:g.67925924C>T	NCBI36
NG_009013.1:g.10104G>A
NG_033043.1:g.1076G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032382.5:c.1413+1G>A MANE Select	NP_115758.3:n.1413+1G>A
ENST00000306875.10:c.1413+1G>A MANE Select	ENSP00000305459.6:n.1413+1G>A
NM_001374871.1:c.1413+1G>A	NP_001361800.1:n.1413+1G>A
NM_001379261.1:c.1413+1G>A	NP_001366190.1:n.1413+1G>A
NM_001379262.1:c.1413+1G>A	NP_001366191.1:n.1413+1G>A
NM_001379263.1:c.1413+1G>A	NP_001366192.1:n.1413+1G>A
NM_001379264.1:c.1413+1G>A	NP_001366193.1:n.1413+1G>A
NM_001379265.1:c.1413+1G>A	NP_001366194.1:n.1413+1G>A
NM_001379266.1:c.1413+1G>A	NP_001366195.1:n.1413+1G>A
NM_032382.4:c.1413+1G>A	NP_115758.3:n.1413+1G>A
ENST00000306875.8:c.1413+1G>A	ENSP00000305459.4:n.1413+1G>A
ENST00000562081.2:c.1413+1G>A	ENSP00000455954.1:n.1413+1G>A
ENST00000562595.5:c.549+806G>A
ENST00000562949.1:c.351+1G>A	ENSP00000457718.1:n.351+1G>A