Canonical Allele Identifier: CA2806368041

Gene: IL4R

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27362898_27362899insGGCATCTCGGGTTCT , CM000678.2:g.27362898_27362899insGGCATCTCGGGTTCT	GRCh38
NC_000016.9:g.27374219_27374220insGGCATCTCGGGTTCT , CM000678.1:g.27374219_27374220insGGCATCTCGGGTTCT	GRCh37
NC_000016.8:g.27281720_27281721insGGCATCTCGGGTTCT	NCBI36
NG_012086.1:g.53969_53970insGGCATCTCGGGTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395762.7:c.1546_1547insGGCATCTCGGGTTCT MANE Select	ENSP00000379111.2:p.Asp516delinsGlyHisLeuGlyPheTyr
ENST00000170630.6:c.1501_1502insGGCATCTCGGGTTCT	ENSP00000170630.3:p.Asp501delinsGlyHisLeuGlyPheTyr
ENST00000395762.6:c.1546_1547insGGCATCTCGGGTTCT	ENSP00000379111.2:p.Asp516delinsGlyHisLeuGlyPheTyr
ENST00000543915.6:c.1546_1547insGGCATCTCGGGTTCT	ENSP00000441667.2:p.Asp516delinsGlyHisLeuGlyPheTyr
ENST00000565352.1:c.230-1205_230-1204insGGCATCTCGGGTTCT	ENSP00000461268.1:n.230-1205_230-1204insGGCATCTCGGGTTCT
ENST00000568746.5:c.*1589_*1590insGGCATCTCGGGTTCT	ENSP00000455714.1:n.*1589_*1590insGGCATCTCGGGTTCT
NM_000418.3:c.1546_1547insGGCATCTCGGGTTCT	NP_000409.1:p.Asp516delinsGlyHisLeuGlyPheTyr
NM_001257406.1:c.1546_1547insGGCATCTCGGGTTCT	NP_001244335.1:p.Asp516delinsGlyHisLeuGlyPheTyr
NM_001257407.1:c.1501_1502insGGCATCTCGGGTTCT	NP_001244336.1:p.Asp501delinsGlyHisLeuGlyPheTyr
NM_001257997.1:c.1066_1067insGGCATCTCGGGTTCT	NP_001244926.1:p.Asp356delinsGlyHisLeuGlyPheTyr
XM_005255308.2:c.655_656insGGCATCTCGGGTTCT	XP_005255365.1:p.Asp219delinsGlyHisLeuGlyPheTyr
XM_006721043.1:c.595_596insGGCATCTCGGGTTCT	XP_006721106.1:p.Asp199delinsGlyHisLeuGlyPheTyr
XM_011545825.1:c.1546_1547insGGCATCTCGGGTTCT	XP_011544127.1:p.Asp516delinsGlyHisLeuGlyPheTyr
XM_011545826.1:c.1546_1547insGGCATCTCGGGTTCT	XP_011544128.1:p.Asp516delinsGlyHisLeuGlyPheTyr
XM_011545827.1:c.1546_1547insGGCATCTCGGGTTCT	XP_011544129.1:p.Asp516delinsGlyHisLeuGlyPheTyr
XM_011545828.1:c.1279_1280insGGCATCTCGGGTTCT	XP_011544130.1:p.Asp427delinsGlyHisLeuGlyPheTyr
XM_011545829.1:c.1249_1250insGGCATCTCGGGTTCT	XP_011544131.1:p.Asp417delinsGlyHisLeuGlyPheTyr
XM_011545830.1:c.1249_1250insGGCATCTCGGGTTCT	XP_011544132.1:p.Asp417delinsGlyHisLeuGlyPheTyr
XM_011545831.1:c.1249_1250insGGCATCTCGGGTTCT	XP_011544133.1:p.Asp417delinsGlyHisLeuGlyPheTyr
XM_011545832.1:c.1249_1250insGGCATCTCGGGTTCT	XP_011544134.1:p.Asp417delinsGlyHisLeuGlyPheTyr
XM_011545833.1:c.1249_1250insGGCATCTCGGGTTCT	XP_011544135.1:p.Asp417delinsGlyHisLeuGlyPheTyr
XM_011545834.1:c.1123_1124insGGCATCTCGGGTTCT	XP_011544136.1:p.Asp375delinsGlyHisLeuGlyPheTyr
XM_011545826.2:c.1546_1547insGGCATCTCGGGTTCT	XP_011544128.1:p.Asp516delinsGlyHisLeuGlyPheTyr
XM_011545827.2:c.1546_1547insGGCATCTCGGGTTCT	XP_011544129.1:p.Asp516delinsGlyHisLeuGlyPheTyr
XM_011545828.2:c.1279_1280insGGCATCTCGGGTTCT	XP_011544130.1:p.Asp427delinsGlyHisLeuGlyPheTyr
XM_011545830.2:c.1249_1250insGGCATCTCGGGTTCT	XP_011544132.1:p.Asp417delinsGlyHisLeuGlyPheTyr
XM_011545833.2:c.1249_1250insGGCATCTCGGGTTCT	XP_011544135.1:p.Asp417delinsGlyHisLeuGlyPheTyr
XM_011545834.2:c.1123_1124insGGCATCTCGGGTTCT	XP_011544136.1:p.Asp375delinsGlyHisLeuGlyPheTyr
NM_000418.4:c.1546_1547insGGCATCTCGGGTTCT MANE Select	NP_000409.1:p.Asp516delinsGlyHisLeuGlyPheTyr
NM_001257406.2:c.1546_1547insGGCATCTCGGGTTCT	NP_001244335.1:p.Asp516delinsGlyHisLeuGlyPheTyr
NM_001257407.2:c.1501_1502insGGCATCTCGGGTTCT	NP_001244336.1:p.Asp501delinsGlyHisLeuGlyPheTyr
NM_001257997.2:c.1066_1067insGGCATCTCGGGTTCT	NP_001244926.1:p.Asp356delinsGlyHisLeuGlyPheTyr