Canonical Allele Identifier: CA395301740
Gene: IL21R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.27442964A>C , CM000678.2:g.27442964A>C GRCh38
NC_000016.9:g.27454285A>C , CM000678.1:g.27454285A>C GRCh37
NC_000016.8:g.27361786A>C NCBI36
NG_012222.1:g.45563A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000697146.1:c.353-3A>C ENSP00000513135.1:n.353-3A>C
ENST00000337929.8:c.355A>C MANE Select ENSP00000338010.3:p.Lys119Gln
ENST00000337929.7:c.355A>C ENSP00000338010.3:p.Lys119Gln
ENST00000395754.4:c.355A>C ENSP00000379103.4:p.Lys119Gln
ENST00000561953.1:n.295A>C
ENST00000564089.5:c.355A>C ENSP00000456707.1:p.Lys119Gln
NM_021798.3:c.355A>C NP_068570.1:p.Lys119Gln
NM_181078.2:c.355A>C NP_851564.1:p.Lys119Gln
NM_181079.4:c.421A>C NP_851565.4:p.Lys141Gln
XM_011545857.1:c.421A>C XP_011544159.1:p.Lys141Gln
XM_011545858.1:c.136-1578A>C XP_011544160.1:n.136-1578A>C
XM_011545857.3:c.421A>C XP_011544159.1:p.Lys141Gln
XM_011545858.3:c.136-1578A>C XP_011544160.1:n.136-1578A>C
XM_017023257.2:c.355A>C XP_016878746.1:p.Lys119Gln
NM_181078.3:c.355A>C MANE Select NP_851564.1:p.Lys119Gln
NM_021798.4:c.355A>C NP_068570.1:p.Lys119Gln
NM_181079.5:c.421A>C NP_851565.4:p.Lys141Gln