Canonical Allele Identifier: CA2646125957

Gene: IL23R

Linked Data

• gnomAD v4: 1-67259211-CTCTTTTTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259212_67259219del , CM000663.2:g.67259212_67259219del	GRCh38
NC_000001.10:g.67724895_67724902del , CM000663.1:g.67724895_67724902del	GRCh37
NC_000001.9:g.67497483_67497490del	NCBI36
NG_011498.1:g.97727_97734del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347310.10:c.*84_*91del MANE Select	ENSP00000321345.5:n.*84_*91del
ENST00000347310.9:c.*84_*91del	ENSP00000321345.5:n.*84_*91del
ENST00000395227.2:c.*84_*91del	ENSP00000378652.2:n.*84_*91del
ENST00000425614.3:c.*84_*91del	ENSP00000387640.2:n.*84_*91del
ENST00000473881.2:c.*800_*807del	ENSP00000486667.1:n.*800_*807del
NM_144701.2:c.*84_*91del	NP_653302.2:n.*84_*91del
XM_005270516.2:c.*84_*91del	XP_005270573.1:n.*84_*91del
XM_011540789.1:c.*84_*91del	XP_011539091.1:n.*84_*91del
XM_011540790.1:c.*84_*91del	XP_011539092.1:n.*84_*91del
XM_011540791.1:c.*84_*91del	XP_011539093.1:n.*84_*91del
XM_011540790.3:c.*84_*91del	XP_011539092.1:n.*84_*91del
XM_011540791.3:c.*84_*91del	XP_011539093.1:n.*84_*91del
NM_144701.3:c.*84_*91del MANE Select	NP_653302.2:n.*84_*91del