Canonical Allele Identifier: CA2540392421
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259305_67259306insAGCTTTCT , CM000663.2:g.67259305_67259306insAGCTTTCT GRCh38
NC_000001.10:g.67724988_67724989insAGCTTTCT , CM000663.1:g.67724988_67724989insAGCTTTCT GRCh37
NC_000001.9:g.67497576_67497577insAGCTTTCT NCBI36
NG_011498.1:g.97820_97821insAGCTTTCT

Transcript Alleles

HGVS Amino-acid change
ENST00000347310.10:c.*177_*178insAGCTTTCT MANE Select ENSP00000321345.5:n.*177_*178insAGCTTTCT
ENST00000347310.9:c.*177_*178insAGCTTTCT ENSP00000321345.5:n.*177_*178insAGCTTTCT
ENST00000395227.2:c.*177_*178insAGCTTTCT ENSP00000378652.2:n.*177_*178insAGCTTTCT
ENST00000473881.2:c.*893_*894insAGCTTTCT ENSP00000486667.1:n.*893_*894insAGCTTTCT
NM_144701.2:c.*177_*178insAGCTTTCT NP_653302.2:n.*177_*178insAGCTTTCT
XM_005270516.2:c.*177_*178insAGCTTTCT XP_005270573.1:n.*177_*178insAGCTTTCT
XM_011540789.1:c.*177_*178insAGCTTTCT XP_011539091.1:n.*177_*178insAGCTTTCT
XM_011540790.1:c.*177_*178insAGCTTTCT XP_011539092.1:n.*177_*178insAGCTTTCT
XM_011540791.1:c.*177_*178insAGCTTTCT XP_011539093.1:n.*177_*178insAGCTTTCT
XM_011540790.3:c.*177_*178insAGCTTTCT XP_011539092.1:n.*177_*178insAGCTTTCT
XM_011540791.3:c.*177_*178insAGCTTTCT XP_011539093.1:n.*177_*178insAGCTTTCT
NM_144701.3:c.*177_*178insAGCTTTCT MANE Select NP_653302.2:n.*177_*178insAGCTTTCT