Canonical Allele Identifier: CA2646126235

Gene: IL23R

Linked Data

• gnomAD v4: 1-67259558-C-CCTG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259558_67259559insCTG , CM000663.2:g.67259558_67259559insCTG	GRCh38
NC_000001.10:g.67725241_67725242insCTG , CM000663.1:g.67725241_67725242insCTG	GRCh37
NC_000001.9:g.67497829_67497830insCTG	NCBI36
NG_011498.1:g.98073_98074insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347310.10:c.*430_*431insCTG MANE Select	ENSP00000321345.5:n.*430_*431insCTG
ENST00000347310.9:c.*430_*431insCTG	ENSP00000321345.5:n.*430_*431insCTG
ENST00000395227.2:c.*430_*431insCTG	ENSP00000378652.2:n.*430_*431insCTG
ENST00000473881.2:c.*1146_*1147insCTG	ENSP00000486667.1:n.*1146_*1147insCTG
NM_144701.2:c.*430_*431insCTG	NP_653302.2:n.*430_*431insCTG
XM_005270516.2:c.*430_*431insCTG	XP_005270573.1:n.*430_*431insCTG
XM_011540789.1:c.*430_*431insCTG	XP_011539091.1:n.*430_*431insCTG
XM_011540790.1:c.*430_*431insCTG	XP_011539092.1:n.*430_*431insCTG
XM_011540791.1:c.*430_*431insCTG	XP_011539093.1:n.*430_*431insCTG
XM_011540790.3:c.*430_*431insCTG	XP_011539092.1:n.*430_*431insCTG
XM_011540791.3:c.*430_*431insCTG	XP_011539093.1:n.*430_*431insCTG
NM_144701.3:c.*430_*431insCTG MANE Select	NP_653302.2:n.*430_*431insCTG