Canonical Allele Identifier: CA2215233673

Gene: IL21R

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27443056_27443057delinsGC , CM000678.2:g.27443056_27443057delinsGC	GRCh38
NC_000016.9:g.27454377_27454378delinsGC , CM000678.1:g.27454377_27454378delinsGC	GRCh37
NC_000016.8:g.27361878_27361879delinsGC	NCBI36
NG_012222.1:g.45655_45656delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697146.1:c.*43_*44delinsGC	ENSP00000513135.1:n.*43_*44delinsGC
ENST00000337929.8:c.447_448delinsGC MANE Select	ENSP00000338010.3:p.Met149=
ENST00000337929.7:c.447_448delinsGC	ENSP00000338010.3:p.Met149=
ENST00000395754.4:c.447_448delinsGC	ENSP00000379103.4:p.Met149=
ENST00000561953.1:n.387_388delinsGC
ENST00000564089.5:c.447_448delinsGC	ENSP00000456707.1:p.Met149=
NM_021798.3:c.447_448delinsGC	NP_068570.1:p.Met149=
NM_181078.2:c.447_448delinsGC	NP_851564.1:p.Met149=
NM_181079.4:c.513_514delinsGC	NP_851565.4:p.Met171=
XM_011545857.1:c.513_514delinsGC	XP_011544159.1:p.Met171=
XM_011545858.1:c.136-1486_136-1485delinsGC	XP_011544160.1:n.136-1486_136-1485delinsGC
XM_011545857.3:c.513_514delinsGC	XP_011544159.1:p.Met171=
XM_011545858.3:c.136-1486_136-1485delinsGC	XP_011544160.1:n.136-1486_136-1485delinsGC
XM_017023257.2:c.447_448delinsGC	XP_016878746.1:p.Met149=
NM_181078.3:c.447_448delinsGC MANE Select	NP_851564.1:p.Met149=
NM_021798.4:c.447_448delinsGC	NP_068570.1:p.Met149=
NM_181079.5:c.513_514delinsGC	NP_851565.4:p.Met171=