Canonical Allele Identifier: CA2215169918

Gene: IL4R

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27362923A= , CM000678.2:g.27362923A=	GRCh38
NC_000016.9:g.27374244A= , CM000678.1:g.27374244A=	GRCh37
NC_000016.8:g.27281745A=	NCBI36
NG_012086.1:g.53994A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395762.7:c.1571A= MANE Select	ENSP00000379111.2:p.Glu524=
ENST00000170630.6:c.1526A=	ENSP00000170630.3:p.Glu509=
ENST00000395762.6:c.1571A=	ENSP00000379111.2:p.Glu524=
ENST00000543915.6:c.1571A=	ENSP00000441667.2:p.Glu524=
ENST00000565352.1:c.230-1180A=	ENSP00000461268.1:n.230-1180A=
ENST00000568746.5:c.*1614A=	ENSP00000455714.1:n.*1614A=
NM_000418.3:c.1571A=	NP_000409.1:p.Glu524=
NM_001257406.1:c.1571A=	NP_001244335.1:p.Glu524=
NM_001257407.1:c.1526A=	NP_001244336.1:p.Glu509=
NM_001257997.1:c.1091A=	NP_001244926.1:p.Glu364=
XM_005255308.2:c.680A=	XP_005255365.1:p.Glu227=
XM_006721043.1:c.620A=	XP_006721106.1:p.Glu207=
XM_011545825.1:c.1571A=	XP_011544127.1:p.Glu524=
XM_011545826.1:c.1571A=	XP_011544128.1:p.Glu524=
XM_011545827.1:c.1571A=	XP_011544129.1:p.Glu524=
XM_011545828.1:c.1304A=	XP_011544130.1:p.Glu435=
XM_011545829.1:c.1274A=	XP_011544131.1:p.Glu425=
XM_011545830.1:c.1274A=	XP_011544132.1:p.Glu425=
XM_011545831.1:c.1274A=	XP_011544133.1:p.Glu425=
XM_011545832.1:c.1274A=	XP_011544134.1:p.Glu425=
XM_011545833.1:c.1274A=	XP_011544135.1:p.Glu425=
XM_011545834.1:c.1148A=	XP_011544136.1:p.Glu383=
XM_011545826.2:c.1571A=	XP_011544128.1:p.Glu524=
XM_011545827.2:c.1571A=	XP_011544129.1:p.Glu524=
XM_011545828.2:c.1304A=	XP_011544130.1:p.Glu435=
XM_011545830.2:c.1274A=	XP_011544132.1:p.Glu425=
XM_011545833.2:c.1274A=	XP_011544135.1:p.Glu425=
XM_011545834.2:c.1148A=	XP_011544136.1:p.Glu383=
NM_000418.4:c.1571A= MANE Select	NP_000409.1:p.Glu524=
NM_001257406.2:c.1571A=	NP_001244335.1:p.Glu524=
NM_001257407.2:c.1526A=	NP_001244336.1:p.Glu509=
NM_001257997.2:c.1091A=	NP_001244926.1:p.Glu364=