Canonical Allele Identifier: CA2386486330
Gene: OLIG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026375_33026387delinsTCCGTTTGAGGAA , CM000683.2:g.33026375_33026387delinsTCCGTTTGAGGAA GRCh38
NC_000021.8:g.34398683_34398695delinsTCCGTTTGAGGAA , CM000683.1:g.34398683_34398695delinsTCCGTTTGAGGAA GRCh37
NC_000021.7:g.33320553_33320565delinsTCCGTTTGAGGAA NCBI36
NG_011834.1:g.5445_5457delinsTCCGTTTGAGGAA

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+349_-63+361delinsTCCGTTTGAGGAA MANE Select ENSP00000371794.3:n.-63+349_-63+361delins...
ENST00000333337.3:c.-488_-476delinsTCCGTTTGAGGAA ENSP00000331040.3:n.-488_-476delinsTCCGTT...
ENST00000382357.3:c.-63+349_-63+361delinsTCCGTTTGAGGAA ENSP00000371794.3:n.-63+349_-63+361delins...
ENST00000430860.1:c.-63+115_-63+127delinsTCCGTTTGAGGAA ENSP00000391183.1:n.-63+115_-63+127delins...
NM_005806.3:c.-63+349_-63+361delinsTCCGTTTGAGGAA NP_005797.1:n.-63+349_-63+361delinsTCCGTT...
XM_005260908.1:c.-63+115_-63+127delinsTCCGTTTGAGGAA XP_005260965.1:n.-63+115_-63+127delinsTCC...
NM_005806.4:c.-63+349_-63+361delinsTCCGTTTGAGGAA MANE Select NP_005797.1:n.-63+349_-63+361delinsTCCGTT...