Canonical Allele Identifier: CA1173064374

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259175_67259187delinsACTTGGGTTTTCC , CM000663.2:g.67259175_67259187delinsACTTGGGTTTTCC	GRCh38
NC_000001.10:g.67724858_67724870delinsACTTGGGTTTTCC , CM000663.1:g.67724858_67724870delinsACTTGGGTTTTCC	GRCh37
NC_000001.9:g.67497446_67497458delinsACTTGGGTTTTCC	NCBI36
NG_011498.1:g.97690_97702delinsACTTGGGTTTTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347310.10:c.*47_*59delinsACTTGGGTTTTCC MANE Select	ENSP00000321345.5:n.*47_*59delinsACTTGGGTTTTCC
ENST00000347310.9:c.*47_*59delinsACTTGGGTTTTCC	ENSP00000321345.5:n.*47_*59delinsACTTGGGTTTTCC
ENST00000395227.2:c.*47_*59delinsACTTGGGTTTTCC	ENSP00000378652.2:n.*47_*59delinsACTTGGGTTTTCC
ENST00000425614.3:c.*47_*59delinsACTTGGGTTTTCC	ENSP00000387640.2:n.*47_*59delinsACTTGGGTTTTCC
ENST00000473881.2:c.*763_*775delinsACTTGGGTTTTCC	ENSP00000486667.1:n.*763_*775delinsACTTGGGTTTTCC
NM_144701.2:c.*47_*59delinsACTTGGGTTTTCC	NP_653302.2:n.*47_*59delinsACTTGGGTTTTCC
XM_005270516.2:c.*47_*59delinsACTTGGGTTTTCC	XP_005270573.1:n.*47_*59delinsACTTGGGTTTTCC
XM_011540789.1:c.*47_*59delinsACTTGGGTTTTCC	XP_011539091.1:n.*47_*59delinsACTTGGGTTTTCC
XM_011540790.1:c.*47_*59delinsACTTGGGTTTTCC	XP_011539092.1:n.*47_*59delinsACTTGGGTTTTCC
XM_011540791.1:c.*47_*59delinsACTTGGGTTTTCC	XP_011539093.1:n.*47_*59delinsACTTGGGTTTTCC
XM_011540790.3:c.*47_*59delinsACTTGGGTTTTCC	XP_011539092.1:n.*47_*59delinsACTTGGGTTTTCC
XM_011540791.3:c.*47_*59delinsACTTGGGTTTTCC	XP_011539093.1:n.*47_*59delinsACTTGGGTTTTCC
NM_144701.3:c.*47_*59delinsACTTGGGTTTTCC MANE Select	NP_653302.2:n.*47_*59delinsACTTGGGTTTTCC