Canonical Allele Identifier: CA621692229

Gene: IL21R

Linked Data

• dbSNP Id: rs1285969939
• gnomAD v2: 16-27454377-GC-G
• gnomAD v4: 16-27443056-GC-G
• MyVariant Identifiers: chr16:g.27454378del (hg19) ; chr16:g.27443057del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27443057del , CM000678.2:g.27443057del	GRCh38
NC_000016.9:g.27454378del , CM000678.1:g.27454378del	GRCh37
NC_000016.8:g.27361879del	NCBI36
NG_012222.1:g.45656del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697146.1:c.*44del	ENSP00000513135.1:n.*44del
ENST00000337929.8:c.448del MANE Select	ENSP00000338010.3:p.Leu150Ter
ENST00000337929.7:c.448del	ENSP00000338010.3:p.Leu150Ter
ENST00000395754.4:c.448del	ENSP00000379103.4:p.Leu150Ter
ENST00000561953.1:n.388del
ENST00000564089.5:c.448del	ENSP00000456707.1:p.Leu150Ter
NM_021798.3:c.448del	NP_068570.1:p.Leu150Ter
NM_181078.2:c.448del	NP_851564.1:p.Leu150Ter
NM_181079.4:c.514del	NP_851565.4:p.Leu172Ter
XM_011545857.1:c.514del	XP_011544159.1:p.Leu172Ter
XM_011545858.1:c.136-1485del	XP_011544160.1:n.136-1485del
XM_011545857.3:c.514del	XP_011544159.1:p.Leu172Ter
XM_011545858.3:c.136-1485del	XP_011544160.1:n.136-1485del
XM_017023257.2:c.448del	XP_016878746.1:p.Leu150Ter
NM_181078.3:c.448del MANE Select	NP_851564.1:p.Leu150Ter
NM_021798.4:c.448del	NP_068570.1:p.Leu150Ter
NM_181079.5:c.514del	NP_851565.4:p.Leu172Ter