Canonical Allele Identifier: CA395301780

Gene: IL21R

Linked Data

• COSMIC: COSM1323617
• MyVariant Identifiers: chr16:g.27454297C>A (hg19) ; chr16:g.27442976C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27442976C>A , CM000678.2:g.27442976C>A	GRCh38
NC_000016.9:g.27454297C>A , CM000678.1:g.27454297C>A	GRCh37
NC_000016.8:g.27361798C>A	NCBI36
NG_012222.1:g.45575C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697146.1:c.362C>A	ENSP00000513135.1:p.Pro121His
ENST00000337929.8:c.367C>A MANE Select	ENSP00000338010.3:p.Pro123Thr
ENST00000337929.7:c.367C>A	ENSP00000338010.3:p.Pro123Thr
ENST00000395754.4:c.367C>A	ENSP00000379103.4:p.Pro123Thr
ENST00000561953.1:n.307C>A
ENST00000564089.5:c.367C>A	ENSP00000456707.1:p.Pro123Thr
NM_021798.3:c.367C>A	NP_068570.1:p.Pro123Thr
NM_181078.2:c.367C>A	NP_851564.1:p.Pro123Thr
NM_181079.4:c.433C>A	NP_851565.4:p.Pro145Thr
XM_011545857.1:c.433C>A	XP_011544159.1:p.Pro145Thr
XM_011545858.1:c.136-1566C>A	XP_011544160.1:n.136-1566C>A
XM_011545857.3:c.433C>A	XP_011544159.1:p.Pro145Thr
XM_011545858.3:c.136-1566C>A	XP_011544160.1:n.136-1566C>A
XM_017023257.2:c.367C>A	XP_016878746.1:p.Pro123Thr
NM_181078.3:c.367C>A MANE Select	NP_851564.1:p.Pro123Thr
NM_021798.4:c.367C>A	NP_068570.1:p.Pro123Thr
NM_181079.5:c.433C>A	NP_851565.4:p.Pro145Thr