Canonical Allele Identifier: CA2575953141

Gene: IL21R

Linked Data

• gnomAD v4: 16-27443147-TGGGAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27443158_27443162del , CM000678.2:g.27443158_27443162del	GRCh38
NC_000016.9:g.27454479_27454483del , CM000678.1:g.27454479_27454483del	GRCh37
NC_000016.8:g.27361980_27361984del	NCBI36
NG_012222.1:g.45757_45761del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697146.1:c.*103+42_*103+46del	ENSP00000513135.1:n.*103+42_*103+46del
ENST00000337929.8:c.507+42_507+46del MANE Select	ENSP00000338010.3:n.507+42_507+46del
ENST00000337929.7:c.507+42_507+46del	ENSP00000338010.3:n.507+42_507+46del
ENST00000395754.4:c.507+42_507+46del	ENSP00000379103.4:n.507+42_507+46del
ENST00000561953.1:n.447+42_447+46del
ENST00000564089.5:c.507+42_507+46del	ENSP00000456707.1:n.507+42_507+46del
NM_021798.3:c.507+42_507+46del	NP_068570.1:n.507+42_507+46del
NM_181078.2:c.507+42_507+46del	NP_851564.1:n.507+42_507+46del
NM_181079.4:c.573+42_573+46del	NP_851565.4:n.573+42_573+46del
XM_011545857.1:c.573+42_573+46del	XP_011544159.1:n.573+42_573+46del
XM_011545858.1:c.136-1384_136-1380del	XP_011544160.1:n.136-1384_136-1380del
XM_011545857.3:c.573+42_573+46del	XP_011544159.1:n.573+42_573+46del
XM_011545858.3:c.136-1384_136-1380del	XP_011544160.1:n.136-1384_136-1380del
XM_017023257.2:c.507+42_507+46del	XP_016878746.1:n.507+42_507+46del
NM_181078.3:c.507+42_507+46del MANE Select	NP_851564.1:n.507+42_507+46del
NM_021798.4:c.507+42_507+46del	NP_068570.1:n.507+42_507+46del
NM_181079.5:c.573+42_573+46del	NP_851565.4:n.573+42_573+46del