Canonical Allele Identifier: CA2215169830

Gene: IL4R

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27362825_27362827delinsCGC , CM000678.2:g.27362825_27362827delinsCGC	GRCh38
NC_000016.9:g.27374146_27374148delinsCGC , CM000678.1:g.27374146_27374148delinsCGC	GRCh37
NC_000016.8:g.27281647_27281649delinsCGC	NCBI36
NG_012086.1:g.53896_53898delinsCGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395762.7:c.1473_1475delinsCGC MANE Select	ENSP00000379111.2:p.Ile491=
ENST00000170630.6:c.1428_1430delinsCGC	ENSP00000170630.3:p.Ile476=
ENST00000395762.6:c.1473_1475delinsCGC	ENSP00000379111.2:p.Ile491=
ENST00000543915.6:c.1473_1475delinsCGC	ENSP00000441667.2:p.Ile491=
ENST00000565352.1:c.230-1278_230-1276delinsCGC	ENSP00000461268.1:n.230-1278_230-1276delinsCGC
ENST00000568746.5:c.*1516_*1518delinsCGC	ENSP00000455714.1:n.*1516_*1518delinsCGC
NM_000418.3:c.1473_1475delinsCGC	NP_000409.1:p.Ile491=
NM_001257406.1:c.1473_1475delinsCGC	NP_001244335.1:p.Ile491=
NM_001257407.1:c.1428_1430delinsCGC	NP_001244336.1:p.Ile476=
NM_001257997.1:c.993_995delinsCGC	NP_001244926.1:p.Ile331=
XM_005255308.2:c.582_584delinsCGC	XP_005255365.1:p.Ile194=
XM_006721043.1:c.522_524delinsCGC	XP_006721106.1:p.Ile174=
XM_011545825.1:c.1473_1475delinsCGC	XP_011544127.1:p.Ile491=
XM_011545826.1:c.1473_1475delinsCGC	XP_011544128.1:p.Ile491=
XM_011545827.1:c.1473_1475delinsCGC	XP_011544129.1:p.Ile491=
XM_011545828.1:c.1206_1208delinsCGC	XP_011544130.1:p.Ile402=
XM_011545829.1:c.1176_1178delinsCGC	XP_011544131.1:p.Ile392=
XM_011545830.1:c.1176_1178delinsCGC	XP_011544132.1:p.Ile392=
XM_011545831.1:c.1176_1178delinsCGC	XP_011544133.1:p.Ile392=
XM_011545832.1:c.1176_1178delinsCGC	XP_011544134.1:p.Ile392=
XM_011545833.1:c.1176_1178delinsCGC	XP_011544135.1:p.Ile392=
XM_011545834.1:c.1050_1052delinsCGC	XP_011544136.1:p.Ile350=
XM_011545826.2:c.1473_1475delinsCGC	XP_011544128.1:p.Ile491=
XM_011545827.2:c.1473_1475delinsCGC	XP_011544129.1:p.Ile491=
XM_011545828.2:c.1206_1208delinsCGC	XP_011544130.1:p.Ile402=
XM_011545830.2:c.1176_1178delinsCGC	XP_011544132.1:p.Ile392=
XM_011545833.2:c.1176_1178delinsCGC	XP_011544135.1:p.Ile392=
XM_011545834.2:c.1050_1052delinsCGC	XP_011544136.1:p.Ile350=
XM_017023211.1:c.*508_*510delinsCGC	XP_016878700.1:n.*508_*510delinsCGC
NM_000418.4:c.1473_1475delinsCGC MANE Select	NP_000409.1:p.Ile491=
NM_001257406.2:c.1473_1475delinsCGC	NP_001244335.1:p.Ile491=
NM_001257407.2:c.1428_1430delinsCGC	NP_001244336.1:p.Ile476=
NM_001257997.2:c.993_995delinsCGC	NP_001244926.1:p.Ile331=