Canonical Allele Identifier: CA494247140

Gene: IL21R

Linked Data

• COSMIC: COSM1377011
• MyVariant Identifiers: chr16:g.27454294del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27442977del , CM000678.2:g.27442977del	GRCh38
NC_000016.9:g.27454298del , CM000678.1:g.27454298del	GRCh37
NC_000016.8:g.27361799del	NCBI36
NG_012222.1:g.45576del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697146.1:c.363del	ENSP00000513135.1:p.Gln123AsnfsTer?
ENST00000337929.8:c.368del MANE Select	ENSP00000338010.3:p.Pro123LeufsTer4
ENST00000337929.7:c.368del	ENSP00000338010.3:p.Pro123LeufsTer4
ENST00000395754.4:c.368del	ENSP00000379103.4:p.Pro123LeufsTer4
ENST00000561953.1:n.308del
ENST00000564089.5:c.368del	ENSP00000456707.1:p.Pro123LeufsTer4
NM_021798.3:c.368del	NP_068570.1:p.Pro123LeufsTer4
NM_181078.2:c.368del	NP_851564.1:p.Pro123LeufsTer4
NM_181079.4:c.434del	NP_851565.4:p.Pro145LeufsTer4
XM_011545857.1:c.434del	XP_011544159.1:p.Pro145LeufsTer4
XM_011545858.1:c.136-1565del	XP_011544160.1:n.136-1565del
XM_011545857.3:c.434del	XP_011544159.1:p.Pro145LeufsTer4
XM_011545858.3:c.136-1565del	XP_011544160.1:n.136-1565del
XM_017023257.2:c.368del	XP_016878746.1:p.Pro123LeufsTer4
NM_181078.3:c.368del MANE Select	NP_851564.1:p.Pro123LeufsTer4
NM_021798.4:c.368del	NP_068570.1:p.Pro123LeufsTer4
NM_181079.5:c.434del	NP_851565.4:p.Pro145LeufsTer4