Canonical Allele Identifier: CA2386486370

Gene: OLIG2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33026444_33026445delinsTC , CM000683.2:g.33026444_33026445delinsTC	GRCh38
NC_000021.8:g.34398752_34398753delinsTC , CM000683.1:g.34398752_34398753delinsTC	GRCh37
NC_000021.7:g.33320622_33320623delinsTC	NCBI36
NG_011834.1:g.5514_5515delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000382357.4:c.-62-357_-62-356delinsTC MANE Select	ENSP00000371794.3:n.-62-357_-62-356delins...
ENST00000333337.3:c.-419_-418delinsTC	ENSP00000331040.3:n.-419_-418delinsTC
ENST00000382357.3:c.-62-357_-62-356delinsTC	ENSP00000371794.3:n.-62-357_-62-356delins...
ENST00000430860.1:c.-63+184_-63+185delinsTC	ENSP00000391183.1:n.-63+184_-63+185delins...
NM_005806.3:c.-62-357_-62-356delinsTC	NP_005797.1:n.-62-357_-62-356delinsTC
XM_005260908.1:c.-63+184_-63+185delinsTC	XP_005260965.1:n.-63+184_-63+185delinsTC
NM_005806.4:c.-62-357_-62-356delinsTC MANE Select	NP_005797.1:n.-62-357_-62-356delinsTC