Canonical Allele Identifier: CA2215233687

Gene: IL21R

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27443094A= , CM000678.2:g.27443094A=	GRCh38
NC_000016.9:g.27454415A= , CM000678.1:g.27454415A=	GRCh37
NC_000016.8:g.27361916A=	NCBI36
NG_012222.1:g.45693A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697146.1:c.*81A=	ENSP00000513135.1:n.*81A=
ENST00000337929.8:c.485A= MANE Select	ENSP00000338010.3:p.Asn162=
ENST00000337929.7:c.485A=	ENSP00000338010.3:p.Asn162=
ENST00000395754.4:c.485A=	ENSP00000379103.4:p.Asn162=
ENST00000561953.1:n.425A=
ENST00000564089.5:c.485A=	ENSP00000456707.1:p.Asn162=
NM_021798.3:c.485A=	NP_068570.1:p.Asn162=
NM_181078.2:c.485A=	NP_851564.1:p.Asn162=
NM_181079.4:c.551A=	NP_851565.4:p.Asn184=
XM_011545857.1:c.551A=	XP_011544159.1:p.Asn184=
XM_011545858.1:c.136-1448A=	XP_011544160.1:n.136-1448A=
XM_011545857.3:c.551A=	XP_011544159.1:p.Asn184=
XM_011545858.3:c.136-1448A=	XP_011544160.1:n.136-1448A=
XM_017023257.2:c.485A=	XP_016878746.1:p.Asn162=
NM_181078.3:c.485A= MANE Select	NP_851564.1:p.Asn162=
NM_021798.4:c.485A=	NP_068570.1:p.Asn162=
NM_181079.5:c.551A=	NP_851565.4:p.Asn184=