Canonical Allele Identifier: CA2806370718
Gene: IL21R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.27443225_27443226insCACCCAAC , CM000678.2:g.27443225_27443226insCACCCAAC GRCh38
NC_000016.9:g.27454546_27454547insCACCCAAC , CM000678.1:g.27454546_27454547insCACCCAAC GRCh37
NC_000016.8:g.27362047_27362048insCACCCAAC NCBI36
NG_012222.1:g.45824_45825insCACCCAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000697146.1:c.*103+109_*103+110insCACCCAAC ENSP00000513135.1:n.*103+109_*103+110insCACCCAAC
ENST00000337929.8:c.507+109_507+110insCACCCAAC MANE Select ENSP00000338010.3:n.507+109_507+110insCACCCAAC
ENST00000337929.7:c.507+109_507+110insCACCCAAC ENSP00000338010.3:n.507+109_507+110insCACCCAAC
ENST00000395754.4:c.507+109_507+110insCACCCAAC ENSP00000379103.4:n.507+109_507+110insCACCCAAC
ENST00000561953.1:n.447+109_447+110insCACCCAAC
ENST00000564089.5:c.507+109_507+110insCACCCAAC ENSP00000456707.1:n.507+109_507+110insCACCCAAC
NM_021798.3:c.507+109_507+110insCACCCAAC NP_068570.1:n.507+109_507+110insCACCCAAC
NM_181078.2:c.507+109_507+110insCACCCAAC NP_851564.1:n.507+109_507+110insCACCCAAC
NM_181079.4:c.573+109_573+110insCACCCAAC NP_851565.4:n.573+109_573+110insCACCCAAC
XM_011545857.1:c.573+109_573+110insCACCCAAC XP_011544159.1:n.573+109_573+110insCACCCAAC
XM_011545858.1:c.136-1317_136-1316insCACCCAAC XP_011544160.1:n.136-1317_136-1316insCACCCAAC
XM_011545857.3:c.573+109_573+110insCACCCAAC XP_011544159.1:n.573+109_573+110insCACCCAAC
XM_011545858.3:c.136-1317_136-1316insCACCCAAC XP_011544160.1:n.136-1317_136-1316insCACCCAAC
XM_017023257.2:c.507+109_507+110insCACCCAAC XP_016878746.1:n.507+109_507+110insCACCCAAC
NM_181078.3:c.507+109_507+110insCACCCAAC MANE Select NP_851564.1:n.507+109_507+110insCACCCAAC
NM_021798.4:c.507+109_507+110insCACCCAAC NP_068570.1:n.507+109_507+110insCACCCAAC
NM_181079.5:c.573+109_573+110insCACCCAAC NP_851565.4:n.573+109_573+110insCACCCAAC