Canonical Allele Identifier: CA2817737829

Gene: OLIG2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33026179dup , CM000683.2:g.33026179dup	GRCh38
NC_000021.8:g.34398487dup , CM000683.1:g.34398487dup	GRCh37
NC_000021.7:g.33320357dup	NCBI36
NG_011834.1:g.5249dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000382357.4:c.-63+153dup MANE Select	ENSP00000371794.3:n.-63+153dup
ENST00000333337.3:c.-684dup	ENSP00000331040.3:n.-684dup
ENST00000382357.3:c.-63+153dup	ENSP00000371794.3:n.-63+153dup
ENST00000430860.1:c.-144dup	ENSP00000391183.1:n.-144dup
NM_005806.3:c.-63+153dup	NP_005797.1:n.-63+153dup
XM_005260908.1:c.-144dup	XP_005260965.1:n.-144dup
NM_005806.4:c.-63+153dup MANE Select	NP_005797.1:n.-63+153dup