Canonical Allele Identifier: CA2842443276

Gene: IL4R

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27362562_27362563insAG , CM000678.2:g.27362562_27362563insAG	GRCh38
NC_000016.9:g.27373883_27373884insAG , CM000678.1:g.27373883_27373884insAG	GRCh37
NC_000016.8:g.27281384_27281385insAG	NCBI36
NG_012086.1:g.53633_53634insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395762.7:c.1210_1211insAG MANE Select	ENSP00000379111.2:p.Ala404GlufsTer4
ENST00000170630.6:c.1165_1166insAG	ENSP00000170630.3:p.Ala389GlufsTer4
ENST00000395762.6:c.1210_1211insAG	ENSP00000379111.2:p.Ala404GlufsTer4
ENST00000543915.6:c.1210_1211insAG	ENSP00000441667.2:p.Ala404GlufsTer4
ENST00000565352.1:c.230-1541_230-1540insAG	ENSP00000461268.1:n.230-1541_230-1540insAG
ENST00000568746.5:c.*1253_*1254insAG	ENSP00000455714.1:n.*1253_*1254insAG
NM_000418.3:c.1210_1211insAG	NP_000409.1:p.Ala404GlufsTer4
NM_001257406.1:c.1210_1211insAG	NP_001244335.1:p.Ala404GlufsTer4
NM_001257407.1:c.1165_1166insAG	NP_001244336.1:p.Ala389GlufsTer4
NM_001257997.1:c.730_731insAG	NP_001244926.1:p.Ala244GlufsTer4
XM_005255308.2:c.319_320insAG	XP_005255365.1:p.Ala107GlufsTer4
XM_006721043.1:c.259_260insAG	XP_006721106.1:p.Ala87GlufsTer4
XM_011545825.1:c.1210_1211insAG	XP_011544127.1:p.Ala404GlufsTer4
XM_011545826.1:c.1210_1211insAG	XP_011544128.1:p.Ala404GlufsTer4
XM_011545827.1:c.1210_1211insAG	XP_011544129.1:p.Ala404GlufsTer4
XM_011545828.1:c.943_944insAG	XP_011544130.1:p.Ala315GlufsTer4
XM_011545829.1:c.913_914insAG	XP_011544131.1:p.Ala305GlufsTer4
XM_011545830.1:c.913_914insAG	XP_011544132.1:p.Ala305GlufsTer4
XM_011545831.1:c.913_914insAG	XP_011544133.1:p.Ala305GlufsTer4
XM_011545832.1:c.913_914insAG	XP_011544134.1:p.Ala305GlufsTer4
XM_011545833.1:c.913_914insAG	XP_011544135.1:p.Ala305GlufsTer4
XM_011545834.1:c.787_788insAG	XP_011544136.1:p.Ala263GlufsTer4
XM_011545826.2:c.1210_1211insAG	XP_011544128.1:p.Ala404GlufsTer4
XM_011545827.2:c.1210_1211insAG	XP_011544129.1:p.Ala404GlufsTer4
XM_011545828.2:c.943_944insAG	XP_011544130.1:p.Ala315GlufsTer4
XM_011545830.2:c.913_914insAG	XP_011544132.1:p.Ala305GlufsTer4
XM_011545833.2:c.913_914insAG	XP_011544135.1:p.Ala305GlufsTer4
XM_011545834.2:c.787_788insAG	XP_011544136.1:p.Ala263GlufsTer4
XM_017023211.1:c.*245_*246insAG	XP_016878700.1:n.*245_*246insAG
NM_000418.4:c.1210_1211insAG MANE Select	NP_000409.1:p.Ala404GlufsTer4
NM_001257406.2:c.1210_1211insAG	NP_001244335.1:p.Ala404GlufsTer4
NM_001257407.2:c.1165_1166insAG	NP_001244336.1:p.Ala389GlufsTer4
NM_001257997.2:c.730_731insAG	NP_001244926.1:p.Ala244GlufsTer4