Canonical Allele Identifier: CA2817737844
Gene: OLIG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026385_33026386insC , CM000683.2:g.33026385_33026386insC GRCh38
NC_000021.8:g.34398693_34398694insC , CM000683.1:g.34398693_34398694insC GRCh37
NC_000021.7:g.33320563_33320564insC NCBI36
NG_011834.1:g.5455_5456insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000382357.4:c.-63+359_-63+360insC MANE Select ENSP00000371794.3:n.-63+359_-63+360insC
ENST00000333337.3:c.-478_-477insC ENSP00000331040.3:n.-478_-477insC
ENST00000382357.3:c.-63+359_-63+360insC ENSP00000371794.3:n.-63+359_-63+360insC
ENST00000430860.1:c.-63+125_-63+126insC ENSP00000391183.1:n.-63+125_-63+126insC
NM_005806.3:c.-63+359_-63+360insC NP_005797.1:n.-63+359_-63+360insC
XM_005260908.1:c.-63+125_-63+126insC XP_005260965.1:n.-63+125_-63+126insC
NM_005806.4:c.-63+359_-63+360insC MANE Select NP_005797.1:n.-63+359_-63+360insC