Canonical Allele Identifier: CA395302159

Gene: IL21R

Linked Data

• MyVariant Identifiers: chr16:g.27454388A>T (hg19) ; chr16:g.27443067A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27443067A>T , CM000678.2:g.27443067A>T	GRCh38
NC_000016.9:g.27454388A>T , CM000678.1:g.27454388A>T	GRCh37
NC_000016.8:g.27361889A>T	NCBI36
NG_012222.1:g.45666A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697146.1:c.*54A>T	ENSP00000513135.1:n.*54A>T
ENST00000337929.8:c.458A>T MANE Select	ENSP00000338010.3:p.Lys153Met
ENST00000337929.7:c.458A>T	ENSP00000338010.3:p.Lys153Met
ENST00000395754.4:c.458A>T	ENSP00000379103.4:p.Lys153Met
ENST00000561953.1:n.398A>T
ENST00000564089.5:c.458A>T	ENSP00000456707.1:p.Lys153Met
NM_021798.3:c.458A>T	NP_068570.1:p.Lys153Met
NM_181078.2:c.458A>T	NP_851564.1:p.Lys153Met
NM_181079.4:c.524A>T	NP_851565.4:p.Lys175Met
XM_011545857.1:c.524A>T	XP_011544159.1:p.Lys175Met
XM_011545858.1:c.136-1475A>T	XP_011544160.1:n.136-1475A>T
XM_011545857.3:c.524A>T	XP_011544159.1:p.Lys175Met
XM_011545858.3:c.136-1475A>T	XP_011544160.1:n.136-1475A>T
XM_017023257.2:c.458A>T	XP_016878746.1:p.Lys153Met
NM_181078.3:c.458A>T MANE Select	NP_851564.1:p.Lys153Met
NM_021798.4:c.458A>T	NP_068570.1:p.Lys153Met
NM_181079.5:c.524A>T	NP_851565.4:p.Lys175Met