Canonical Allele Identifier: CA2215169906

Gene: IL4R

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27362894_27362910delinsTCCAGACCCACTGCTGG , CM000678.2:g.27362894_27362910delinsTCCAGACCCACTGCTGG	GRCh38
NC_000016.9:g.27374215_27374231delinsTCCAGACCCACTGCTGG , CM000678.1:g.27374215_27374231delinsTCCAGACCCACTGCTGG	GRCh37
NC_000016.8:g.27281716_27281732delinsTCCAGACCCACTGCTGG	NCBI36
NG_012086.1:g.53965_53981delinsTCCAGACCCACTGCTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395762.7:c.1542_1558delinsTCCAGACCCACTGCTGG MANE Select	ENSP00000379111.2:p.Gly514=
ENST00000170630.6:c.1497_1513delinsTCCAGACCCACTGCTGG	ENSP00000170630.3:p.Gly499=
ENST00000395762.6:c.1542_1558delinsTCCAGACCCACTGCTGG	ENSP00000379111.2:p.Gly514=
ENST00000543915.6:c.1542_1558delinsTCCAGACCCACTGCTGG	ENSP00000441667.2:p.Gly514=
ENST00000565352.1:c.230-1209_230-1193delinsTCCAGACCCACTGCTGG	ENSP00000461268.1:n.230-1209_230-1193delinsTCCAGACCCACTGCTGG
ENST00000568746.5:c.*1585_*1601delinsTCCAGACCCACTGCTGG	ENSP00000455714.1:n.*1585_*1601delinsTCCAGACCCACTGCTGG
NM_000418.3:c.1542_1558delinsTCCAGACCCACTGCTGG	NP_000409.1:p.Gly514=
NM_001257406.1:c.1542_1558delinsTCCAGACCCACTGCTGG	NP_001244335.1:p.Gly514=
NM_001257407.1:c.1497_1513delinsTCCAGACCCACTGCTGG	NP_001244336.1:p.Gly499=
NM_001257997.1:c.1062_1078delinsTCCAGACCCACTGCTGG	NP_001244926.1:p.Gly354=
XM_005255308.2:c.651_667delinsTCCAGACCCACTGCTGG	XP_005255365.1:p.Gly217=
XM_006721043.1:c.591_607delinsTCCAGACCCACTGCTGG	XP_006721106.1:p.Gly197=
XM_011545825.1:c.1542_1558delinsTCCAGACCCACTGCTGG	XP_011544127.1:p.Gly514=
XM_011545826.1:c.1542_1558delinsTCCAGACCCACTGCTGG	XP_011544128.1:p.Gly514=
XM_011545827.1:c.1542_1558delinsTCCAGACCCACTGCTGG	XP_011544129.1:p.Gly514=
XM_011545828.1:c.1275_1291delinsTCCAGACCCACTGCTGG	XP_011544130.1:p.Gly425=
XM_011545829.1:c.1245_1261delinsTCCAGACCCACTGCTGG	XP_011544131.1:p.Gly415=
XM_011545830.1:c.1245_1261delinsTCCAGACCCACTGCTGG	XP_011544132.1:p.Gly415=
XM_011545831.1:c.1245_1261delinsTCCAGACCCACTGCTGG	XP_011544133.1:p.Gly415=
XM_011545832.1:c.1245_1261delinsTCCAGACCCACTGCTGG	XP_011544134.1:p.Gly415=
XM_011545833.1:c.1245_1261delinsTCCAGACCCACTGCTGG	XP_011544135.1:p.Gly415=
XM_011545834.1:c.1119_1135delinsTCCAGACCCACTGCTGG	XP_011544136.1:p.Gly373=
XM_011545826.2:c.1542_1558delinsTCCAGACCCACTGCTGG	XP_011544128.1:p.Gly514=
XM_011545827.2:c.1542_1558delinsTCCAGACCCACTGCTGG	XP_011544129.1:p.Gly514=
XM_011545828.2:c.1275_1291delinsTCCAGACCCACTGCTGG	XP_011544130.1:p.Gly425=
XM_011545830.2:c.1245_1261delinsTCCAGACCCACTGCTGG	XP_011544132.1:p.Gly415=
XM_011545833.2:c.1245_1261delinsTCCAGACCCACTGCTGG	XP_011544135.1:p.Gly415=
XM_011545834.2:c.1119_1135delinsTCCAGACCCACTGCTGG	XP_011544136.1:p.Gly373=
NM_000418.4:c.1542_1558delinsTCCAGACCCACTGCTGG MANE Select	NP_000409.1:p.Gly514=
NM_001257406.2:c.1542_1558delinsTCCAGACCCACTGCTGG	NP_001244335.1:p.Gly514=
NM_001257407.2:c.1497_1513delinsTCCAGACCCACTGCTGG	NP_001244336.1:p.Gly499=
NM_001257997.2:c.1062_1078delinsTCCAGACCCACTGCTGG	NP_001244926.1:p.Gly354=