Canonical Allele Identifier: CA2215233752

Gene: IL21R

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27443217_27443220delinsTGGC , CM000678.2:g.27443217_27443220delinsTGGC	GRCh38
NC_000016.9:g.27454538_27454541delinsTGGC , CM000678.1:g.27454538_27454541delinsTGGC	GRCh37
NC_000016.8:g.27362039_27362042delinsTGGC	NCBI36
NG_012222.1:g.45816_45819delinsTGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697146.1:c.*103+101_*103+104delinsTGGC	ENSP00000513135.1:n.*103+101_*103+104delinsTGGC
ENST00000337929.8:c.507+101_507+104delinsTGGC MANE Select	ENSP00000338010.3:n.507+101_507+104delinsTGGC
ENST00000337929.7:c.507+101_507+104delinsTGGC	ENSP00000338010.3:n.507+101_507+104delinsTGGC
ENST00000395754.4:c.507+101_507+104delinsTGGC	ENSP00000379103.4:n.507+101_507+104delinsTGGC
ENST00000561953.1:n.447+101_447+104delinsTGGC
ENST00000564089.5:c.507+101_507+104delinsTGGC	ENSP00000456707.1:n.507+101_507+104delinsTGGC
NM_021798.3:c.507+101_507+104delinsTGGC	NP_068570.1:n.507+101_507+104delinsTGGC
NM_181078.2:c.507+101_507+104delinsTGGC	NP_851564.1:n.507+101_507+104delinsTGGC
NM_181079.4:c.573+101_573+104delinsTGGC	NP_851565.4:n.573+101_573+104delinsTGGC
XM_011545857.1:c.573+101_573+104delinsTGGC	XP_011544159.1:n.573+101_573+104delinsTGGC
XM_011545858.1:c.136-1325_136-1322delinsTGGC	XP_011544160.1:n.136-1325_136-1322delinsTGGC
XM_011545857.3:c.573+101_573+104delinsTGGC	XP_011544159.1:n.573+101_573+104delinsTGGC
XM_011545858.3:c.136-1325_136-1322delinsTGGC	XP_011544160.1:n.136-1325_136-1322delinsTGGC
XM_017023257.2:c.507+101_507+104delinsTGGC	XP_016878746.1:n.507+101_507+104delinsTGGC
NM_181078.3:c.507+101_507+104delinsTGGC MANE Select	NP_851564.1:n.507+101_507+104delinsTGGC
NM_021798.4:c.507+101_507+104delinsTGGC	NP_068570.1:n.507+101_507+104delinsTGGC
NM_181079.5:c.573+101_573+104delinsTGGC	NP_851565.4:n.573+101_573+104delinsTGGC