Canonical Allele Identifier: CA395302426

Gene: IL21R

Linked Data

• COSMIC: COSM6195148
• MyVariant Identifiers: chr16:g.27454433C>T (hg19) ; chr16:g.27443112C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27443112C>T , CM000678.2:g.27443112C>T	GRCh38
NC_000016.9:g.27454433C>T , CM000678.1:g.27454433C>T	GRCh37
NC_000016.8:g.27361934C>T	NCBI36
NG_012222.1:g.45711C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697146.1:c.*99C>T	ENSP00000513135.1:n.*99C>T
ENST00000337929.8:c.503C>T MANE Select	ENSP00000338010.3:p.Ala168Val
ENST00000337929.7:c.503C>T	ENSP00000338010.3:p.Ala168Val
ENST00000395754.4:c.503C>T	ENSP00000379103.4:p.Ala168Val
ENST00000561953.1:n.443C>T
ENST00000564089.5:c.503C>T	ENSP00000456707.1:p.Ala168Val
NM_021798.3:c.503C>T	NP_068570.1:p.Ala168Val
NM_181078.2:c.503C>T	NP_851564.1:p.Ala168Val
NM_181079.4:c.569C>T	NP_851565.4:p.Ala190Val
XM_011545857.1:c.569C>T	XP_011544159.1:p.Ala190Val
XM_011545858.1:c.136-1430C>T	XP_011544160.1:n.136-1430C>T
XM_011545857.3:c.569C>T	XP_011544159.1:p.Ala190Val
XM_011545858.3:c.136-1430C>T	XP_011544160.1:n.136-1430C>T
XM_017023257.2:c.503C>T	XP_016878746.1:p.Ala168Val
NM_181078.3:c.503C>T MANE Select	NP_851564.1:p.Ala168Val
NM_021798.4:c.503C>T	NP_068570.1:p.Ala168Val
NM_181079.5:c.569C>T	NP_851565.4:p.Ala190Val