Canonical Allele Identifier: CA2654283751
Gene: OLIG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026408_33026409del , CM000683.2:g.33026408_33026409del GRCh38
NC_000021.8:g.34398716_34398717del , CM000683.1:g.34398716_34398717del GRCh37
NC_000021.7:g.33320586_33320587del NCBI36
NG_011834.1:g.5478_5479del

Transcript Alleles

HGVS Amino-acid Change
ENST00000382357.4:c.-63+382_-63+383del MANE Select ENSP00000371794.3:n.-63+382_-63+383del
ENST00000333337.3:c.-455_-454del ENSP00000331040.3:n.-455_-454del
ENST00000382357.3:c.-63+382_-63+383del ENSP00000371794.3:n.-63+382_-63+383del
ENST00000430860.1:c.-63+148_-63+149del ENSP00000391183.1:n.-63+148_-63+149del
NM_005806.3:c.-63+382_-63+383del NP_005797.1:n.-63+382_-63+383del
XM_005260908.1:c.-63+148_-63+149del XP_005260965.1:n.-63+148_-63+149del
NM_005806.4:c.-63+382_-63+383del MANE Select NP_005797.1:n.-63+382_-63+383del