Canonical Allele Identifier: CA7975082

Gene: IL21R

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27446045G>A , CM000678.2:g.27446045G>A	GRCh38
NC_000016.9:g.27457366G>A , CM000678.1:g.27457366G>A	GRCh37
NC_000016.8:g.27364867G>A	NCBI36
NG_012222.1:g.48644G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697146.1:c.*420G>A	ENSP00000513135.1:n.*420G>A
ENST00000337929.8:c.824G>A MANE Select	ENSP00000338010.3:p.Arg275Gln
ENST00000337929.7:c.824G>A	ENSP00000338010.3:p.Arg275Gln
ENST00000395754.4:c.824G>A	ENSP00000379103.4:p.Arg275Gln
ENST00000564089.5:c.824G>A	ENSP00000456707.1:p.Arg275Gln
ENST00000564583.1:n.382G>A
NM_021798.3:c.824G>A	NP_068570.1:p.Arg275Gln
NM_181078.2:c.824G>A	NP_851564.1:p.Arg275Gln
NM_181079.4:c.890G>A	NP_851565.4:p.Arg297Gln
XM_011545857.1:c.890G>A	XP_011544159.1:p.Arg297Gln
XM_011545858.1:c.452G>A	XP_011544160.1:p.Arg151Gln
XM_011545857.3:c.890G>A	XP_011544159.1:p.Arg297Gln
XM_011545858.3:c.452G>A	XP_011544160.1:p.Arg151Gln
XM_017023257.2:c.824G>A	XP_016878746.1:p.Arg275Gln
NM_181078.3:c.824G>A MANE Select	NP_851564.1:p.Arg275Gln
NM_021798.4:c.824G>A	NP_068570.1:p.Arg275Gln
NM_181079.5:c.890G>A	NP_851565.4:p.Arg297Gln