Canonical Allele Identifier: CA2215169800

Gene: IL4R

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27362805A= , CM000678.2:g.27362805A=	GRCh38
NC_000016.9:g.27374126A= , CM000678.1:g.27374126A=	GRCh37
NC_000016.8:g.27281627A=	NCBI36
NG_012086.1:g.53876A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395762.7:c.1453A= MANE Select	ENSP00000379111.2:p.Thr485=
ENST00000170630.6:c.1408A=	ENSP00000170630.3:p.Thr470=
ENST00000395762.6:c.1453A=	ENSP00000379111.2:p.Thr485=
ENST00000543915.6:c.1453A=	ENSP00000441667.2:p.Thr485=
ENST00000565352.1:c.230-1298A=	ENSP00000461268.1:n.230-1298A=
ENST00000568746.5:c.*1496A=	ENSP00000455714.1:n.*1496A=
NM_000418.3:c.1453A=	NP_000409.1:p.Thr485=
NM_001257406.1:c.1453A=	NP_001244335.1:p.Thr485=
NM_001257407.1:c.1408A=	NP_001244336.1:p.Thr470=
NM_001257997.1:c.973A=	NP_001244926.1:p.Thr325=
XM_005255308.2:c.562A=	XP_005255365.1:p.Thr188=
XM_006721043.1:c.502A=	XP_006721106.1:p.Thr168=
XM_011545825.1:c.1453A=	XP_011544127.1:p.Thr485=
XM_011545826.1:c.1453A=	XP_011544128.1:p.Thr485=
XM_011545827.1:c.1453A=	XP_011544129.1:p.Thr485=
XM_011545828.1:c.1186A=	XP_011544130.1:p.Thr396=
XM_011545829.1:c.1156A=	XP_011544131.1:p.Thr386=
XM_011545830.1:c.1156A=	XP_011544132.1:p.Thr386=
XM_011545831.1:c.1156A=	XP_011544133.1:p.Thr386=
XM_011545832.1:c.1156A=	XP_011544134.1:p.Thr386=
XM_011545833.1:c.1156A=	XP_011544135.1:p.Thr386=
XM_011545834.1:c.1030A=	XP_011544136.1:p.Thr344=
XM_011545826.2:c.1453A=	XP_011544128.1:p.Thr485=
XM_011545827.2:c.1453A=	XP_011544129.1:p.Thr485=
XM_011545828.2:c.1186A=	XP_011544130.1:p.Thr396=
XM_011545830.2:c.1156A=	XP_011544132.1:p.Thr386=
XM_011545833.2:c.1156A=	XP_011544135.1:p.Thr386=
XM_011545834.2:c.1030A=	XP_011544136.1:p.Thr344=
XM_017023211.1:c.*488A=	XP_016878700.1:n.*488A=
NM_000418.4:c.1453A= MANE Select	NP_000409.1:p.Thr485=
NM_001257406.2:c.1453A=	NP_001244335.1:p.Thr485=
NM_001257407.2:c.1408A=	NP_001244336.1:p.Thr470=
NM_001257997.2:c.973A=	NP_001244926.1:p.Thr325=