Canonical Allele Identifier: CA2991933757

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259217_67259218dup , CM000663.2:g.67259217_67259218dup	GRCh38
NC_000001.10:g.67724900_67724901dup , CM000663.1:g.67724900_67724901dup	GRCh37
NC_000001.9:g.67497488_67497489dup	NCBI36
NG_011498.1:g.97732_97733dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347310.10:c.*89_*90dup MANE Select	ENSP00000321345.5:n.*89_*90dup
ENST00000347310.9:c.*89_*90dup	ENSP00000321345.5:n.*89_*90dup
ENST00000395227.2:c.*89_*90dup	ENSP00000378652.2:n.*89_*90dup
ENST00000425614.3:c.*89_*90dup	ENSP00000387640.2:n.*89_*90dup
ENST00000473881.2:c.*805_*806dup	ENSP00000486667.1:n.*805_*806dup
NM_144701.2:c.*89_*90dup	NP_653302.2:n.*89_*90dup
XM_005270516.2:c.*89_*90dup	XP_005270573.1:n.*89_*90dup
XM_011540789.1:c.*89_*90dup	XP_011539091.1:n.*89_*90dup
XM_011540790.1:c.*89_*90dup	XP_011539092.1:n.*89_*90dup
XM_011540791.1:c.*89_*90dup	XP_011539093.1:n.*89_*90dup
XM_011540790.3:c.*89_*90dup	XP_011539092.1:n.*89_*90dup
XM_011540791.3:c.*89_*90dup	XP_011539093.1:n.*89_*90dup
NM_144701.3:c.*89_*90dup MANE Select	NP_653302.2:n.*89_*90dup