Canonical Allele Identifier: CA2386486318

Gene: OLIG2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33026349_33026352delinsCGTG , CM000683.2:g.33026349_33026352delinsCGTG	GRCh38
NC_000021.8:g.34398657_34398660delinsCGTG , CM000683.1:g.34398657_34398660delinsCGTG	GRCh37
NC_000021.7:g.33320527_33320530delinsCGTG	NCBI36
NG_011834.1:g.5419_5422delinsCGTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000382357.4:c.-63+323_-63+326delinsCGTG MANE Select	ENSP00000371794.3:n.-63+323_-63+326delins...
ENST00000333337.3:c.-514_-511delinsCGTG	ENSP00000331040.3:n.-514_-511delinsCGTG
ENST00000382357.3:c.-63+323_-63+326delinsCGTG	ENSP00000371794.3:n.-63+323_-63+326delins...
ENST00000430860.1:c.-63+89_-63+92delinsCGTG	ENSP00000391183.1:n.-63+89_-63+92delinsCG...
NM_005806.3:c.-63+323_-63+326delinsCGTG	NP_005797.1:n.-63+323_-63+326delinsCGTG
XM_005260908.1:c.-63+89_-63+92delinsCGTG	XP_005260965.1:n.-63+89_-63+92delinsCGTG
NM_005806.4:c.-63+323_-63+326delinsCGTG MANE Select	NP_005797.1:n.-63+323_-63+326delinsCGTG