Canonical Allele Identifier: CA2817737837

Gene: OLIG2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33026331del , CM000683.2:g.33026331del	GRCh38
NC_000021.8:g.34398639del , CM000683.1:g.34398639del	GRCh37
NC_000021.7:g.33320509del	NCBI36
NG_011834.1:g.5401del

Transcript Alleles

HGVS	Amino-acid change
ENST00000382357.4:c.-63+305del MANE Select	ENSP00000371794.3:n.-63+305del
ENST00000333337.3:c.-532del	ENSP00000331040.3:n.-532del
ENST00000382357.3:c.-63+305del	ENSP00000371794.3:n.-63+305del
ENST00000430860.1:c.-63+71del	ENSP00000391183.1:n.-63+71del
NM_005806.3:c.-63+305del	NP_005797.1:n.-63+305del
XM_005260908.1:c.-63+71del	XP_005260965.1:n.-63+71del
NM_005806.4:c.-63+305del MANE Select	NP_005797.1:n.-63+305del