Canonical Allele Identifier: CA2215169862

Gene: IL4R

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27362844C= , CM000678.2:g.27362844C=	GRCh38
NC_000016.9:g.27374165C= , CM000678.1:g.27374165C=	GRCh37
NC_000016.8:g.27281666C=	NCBI36
NG_012086.1:g.53915C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395762.7:c.1492C= MANE Select	ENSP00000379111.2:p.Arg498=
ENST00000170630.6:c.1447C=	ENSP00000170630.3:p.Arg483=
ENST00000395762.6:c.1492C=	ENSP00000379111.2:p.Arg498=
ENST00000543915.6:c.1492C=	ENSP00000441667.2:p.Arg498=
ENST00000565352.1:c.230-1259C=	ENSP00000461268.1:n.230-1259C=
ENST00000568746.5:c.*1535C=	ENSP00000455714.1:n.*1535C=
NM_000418.3:c.1492C=	NP_000409.1:p.Arg498=
NM_001257406.1:c.1492C=	NP_001244335.1:p.Arg498=
NM_001257407.1:c.1447C=	NP_001244336.1:p.Arg483=
NM_001257997.1:c.1012C=	NP_001244926.1:p.Arg338=
XM_005255308.2:c.601C=	XP_005255365.1:p.Arg201=
XM_006721043.1:c.541C=	XP_006721106.1:p.Arg181=
XM_011545825.1:c.1492C=	XP_011544127.1:p.Arg498=
XM_011545826.1:c.1492C=	XP_011544128.1:p.Arg498=
XM_011545827.1:c.1492C=	XP_011544129.1:p.Arg498=
XM_011545828.1:c.1225C=	XP_011544130.1:p.Arg409=
XM_011545829.1:c.1195C=	XP_011544131.1:p.Arg399=
XM_011545830.1:c.1195C=	XP_011544132.1:p.Arg399=
XM_011545831.1:c.1195C=	XP_011544133.1:p.Arg399=
XM_011545832.1:c.1195C=	XP_011544134.1:p.Arg399=
XM_011545833.1:c.1195C=	XP_011544135.1:p.Arg399=
XM_011545834.1:c.1069C=	XP_011544136.1:p.Arg357=
XM_011545826.2:c.1492C=	XP_011544128.1:p.Arg498=
XM_011545827.2:c.1492C=	XP_011544129.1:p.Arg498=
XM_011545828.2:c.1225C=	XP_011544130.1:p.Arg409=
XM_011545830.2:c.1195C=	XP_011544132.1:p.Arg399=
XM_011545833.2:c.1195C=	XP_011544135.1:p.Arg399=
XM_011545834.2:c.1069C=	XP_011544136.1:p.Arg357=
XM_017023211.1:c.*527C=	XP_016878700.1:n.*527C=
NM_000418.4:c.1492C= MANE Select	NP_000409.1:p.Arg498=
NM_001257406.2:c.1492C=	NP_001244335.1:p.Arg498=
NM_001257407.2:c.1447C=	NP_001244336.1:p.Arg483=
NM_001257997.2:c.1012C=	NP_001244926.1:p.Arg338=