Canonical Allele Identifier: CA2386486378

Gene: OLIG2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33026462_33026463delinsGC , CM000683.2:g.33026462_33026463delinsGC	GRCh38
NC_000021.8:g.34398770_34398771delinsGC , CM000683.1:g.34398770_34398771delinsGC	GRCh37
NC_000021.7:g.33320640_33320641delinsGC	NCBI36
NG_011834.1:g.5532_5533delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000382357.4:c.-62-339_-62-338delinsGC MANE Select	ENSP00000371794.3:n.-62-339_-62-338delins...
ENST00000333337.3:c.-401_-400delinsGC	ENSP00000331040.3:n.-401_-400delinsGC
ENST00000382357.3:c.-62-339_-62-338delinsGC	ENSP00000371794.3:n.-62-339_-62-338delins...
ENST00000430860.1:c.-63+202_-63+203delinsGC	ENSP00000391183.1:n.-63+202_-63+203delins...
NM_005806.3:c.-62-339_-62-338delinsGC	NP_005797.1:n.-62-339_-62-338delinsGC
XM_005260908.1:c.-63+202_-63+203delinsGC	XP_005260965.1:n.-63+202_-63+203delinsGC
NM_005806.4:c.-62-339_-62-338delinsGC MANE Select	NP_005797.1:n.-62-339_-62-338delinsGC