Canonical Allele Identifier: CA1139664612

Gene: IL21R

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27444512_27444522del , CM000678.2:g.27444512_27444522del	GRCh38
NC_000016.9:g.27455833_27455843del , CM000678.1:g.27455833_27455843del	GRCh37
NC_000016.8:g.27363334_27363344del	NCBI36
NG_012222.1:g.47111_47121del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697146.1:c.*104-30_*104-20del	ENSP00000513135.1:n.*104-30_*104-20del
ENST00000337929.8:c.508-30_508-20del MANE Select	ENSP00000338010.3:n.508-30_508-20del
ENST00000337929.7:c.508-30_508-20del	ENSP00000338010.3:n.508-30_508-20del
ENST00000395754.4:c.508-30_508-20del	ENSP00000379103.4:n.508-30_508-20del
ENST00000561953.1:n.448-30_448-20del
ENST00000564089.5:c.508-30_508-20del	ENSP00000456707.1:n.508-30_508-20del
ENST00000564583.1:n.68-30_68-20del
NM_021798.3:c.508-30_508-20del	NP_068570.1:n.508-30_508-20del
NM_181078.2:c.508-30_508-20del	NP_851564.1:n.508-30_508-20del
NM_181079.4:c.574-30_574-20del	NP_851565.4:n.574-30_574-20del
XM_011545857.1:c.574-30_574-20del	XP_011544159.1:n.574-30_574-20del
XM_011545858.1:c.136-30_136-20del	XP_011544160.1:n.136-30_136-20del
XM_011545857.3:c.574-30_574-20del	XP_011544159.1:n.574-30_574-20del
XM_011545858.3:c.136-30_136-20del	XP_011544160.1:n.136-30_136-20del
XM_017023257.2:c.508-30_508-20del	XP_016878746.1:n.508-30_508-20del
NM_181078.3:c.508-30_508-20del MANE Select	NP_851564.1:n.508-30_508-20del
NM_021798.4:c.508-30_508-20del	NP_068570.1:n.508-30_508-20del
NM_181079.5:c.574-30_574-20del	NP_851565.4:n.574-30_574-20del