Canonical Allele Identifier: CA2215225372

Gene: IL21R

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27429509T= , CM000678.2:g.27429509T=	GRCh38
NC_000016.9:g.27440830T= , CM000678.1:g.27440830T=	GRCh37
NC_000016.8:g.27348331T=	NCBI36
NG_012222.1:g.32108T=

Transcript Alleles

HGVS	Amino-acid Change
NM_181078.3:c.-16-547T= MANE Select	NP_851564.1:n.-16-547T=
ENST00000337929.8:c.-16-547T= MANE Select	ENSP00000338010.3:n.-16-547T=
NM_021798.3:c.-16-547T=	NP_068570.1:n.-16-547T=
NM_021798.4:c.-16-547T=	NP_068570.1:n.-16-547T=
NM_181078.2:c.-16-547T=	NP_851564.1:n.-16-547T=
NM_181079.4:c.51-547T=	NP_851565.4:n.51-547T=
NM_181079.5:c.51-547T=	NP_851565.4:n.51-547T=
ENST00000337929.7:c.-16-547T=	ENSP00000338010.3:n.-16-547T=
ENST00000395754.4:c.-16-547T=	ENSP00000379103.4:n.-16-547T=
ENST00000564089.5:c.-16-547T=	ENSP00000456707.1:n.-16-547T=
XM_011545857.1:c.51-547T=	XP_011544159.1:n.51-547T=
XM_011545857.3:c.51-547T=	XP_011544159.1:n.51-547T=
XM_011545858.1:c.-233-547T=	XP_011544160.1:n.-233-547T=
XM_011545858.3:c.-233-547T=	XP_011544160.1:n.-233-547T=
XM_017023257.2:c.-16-547T=	XP_016878746.1:n.-16-547T=