Canonical Allele Identifier: CA2654283489

Gene: OLIG2

Linked Data

• gnomAD v4: 21-33026151-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33026154_33026155del , CM000683.2:g.33026154_33026155del	GRCh38
NC_000021.8:g.34398462_34398463del , CM000683.1:g.34398462_34398463del	GRCh37
NC_000021.7:g.33320332_33320333del	NCBI36
NG_011834.1:g.5224_5225del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382357.4:c.-63+128_-63+129del MANE Select	ENSP00000371794.3:n.-63+128_-63+129del
ENST00000333337.3:c.-709_-708del	ENSP00000331040.3:n.-709_-708del
ENST00000382357.3:c.-63+128_-63+129del	ENSP00000371794.3:n.-63+128_-63+129del
ENST00000430860.1:c.-169_-168del	ENSP00000391183.1:n.-169_-168del
NM_005806.3:c.-63+128_-63+129del	NP_005797.1:n.-63+128_-63+129del
XM_005260908.1:c.-169_-168del	XP_005260965.1:n.-169_-168del
NM_005806.4:c.-63+128_-63+129del MANE Select	NP_005797.1:n.-63+128_-63+129del