Canonical Allele Identifier: CA2215169394

Gene: IL4R

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27362455_27362456delinsCG , CM000678.2:g.27362455_27362456delinsCG	GRCh38
NC_000016.9:g.27373776_27373777delinsCG , CM000678.1:g.27373776_27373777delinsCG	GRCh37
NC_000016.8:g.27281277_27281278delinsCG	NCBI36
NG_012086.1:g.53526_53527delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395762.7:c.1103_1104delinsCG MANE Select	ENSP00000379111.2:p.Pro368=
ENST00000170630.6:c.1058_1059delinsCG	ENSP00000170630.3:p.Pro353=
ENST00000395762.6:c.1103_1104delinsCG	ENSP00000379111.2:p.Pro368=
ENST00000543915.6:c.1103_1104delinsCG	ENSP00000441667.2:p.Pro368=
ENST00000565352.1:c.230-1648_230-1647delinsCG	ENSP00000461268.1:n.230-1648_230-1647delinsCG
ENST00000565915.5:n.513_514delinsCG
ENST00000568746.5:c.*1146_*1147delinsCG	ENSP00000455714.1:n.*1146_*1147delinsCG
NM_000418.3:c.1103_1104delinsCG	NP_000409.1:p.Pro368=
NM_001257406.1:c.1103_1104delinsCG	NP_001244335.1:p.Pro368=
NM_001257407.1:c.1058_1059delinsCG	NP_001244336.1:p.Pro353=
NM_001257997.1:c.623_624delinsCG	NP_001244926.1:p.Pro208=
XM_005255308.2:c.212_213delinsCG	XP_005255365.1:p.Pro71=
XM_006721043.1:c.152_153delinsCG	XP_006721106.1:p.Pro51=
XM_011545825.1:c.1103_1104delinsCG	XP_011544127.1:p.Pro368=
XM_011545826.1:c.1103_1104delinsCG	XP_011544128.1:p.Pro368=
XM_011545827.1:c.1103_1104delinsCG	XP_011544129.1:p.Pro368=
XM_011545828.1:c.836_837delinsCG	XP_011544130.1:p.Pro279=
XM_011545829.1:c.806_807delinsCG	XP_011544131.1:p.Pro269=
XM_011545830.1:c.806_807delinsCG	XP_011544132.1:p.Pro269=
XM_011545831.1:c.806_807delinsCG	XP_011544133.1:p.Pro269=
XM_011545832.1:c.806_807delinsCG	XP_011544134.1:p.Pro269=
XM_011545833.1:c.806_807delinsCG	XP_011544135.1:p.Pro269=
XM_011545834.1:c.680_681delinsCG	XP_011544136.1:p.Pro227=
XM_011545826.2:c.1103_1104delinsCG	XP_011544128.1:p.Pro368=
XM_011545827.2:c.1103_1104delinsCG	XP_011544129.1:p.Pro368=
XM_011545828.2:c.836_837delinsCG	XP_011544130.1:p.Pro279=
XM_011545830.2:c.806_807delinsCG	XP_011544132.1:p.Pro269=
XM_011545833.2:c.806_807delinsCG	XP_011544135.1:p.Pro269=
XM_011545834.2:c.680_681delinsCG	XP_011544136.1:p.Pro227=
XM_017023211.1:c.*138_*139delinsCG	XP_016878700.1:n.*138_*139delinsCG
NM_000418.4:c.1103_1104delinsCG MANE Select	NP_000409.1:p.Pro368=
NM_001257406.2:c.1103_1104delinsCG	NP_001244335.1:p.Pro368=
NM_001257407.2:c.1058_1059delinsCG	NP_001244336.1:p.Pro353=
NM_001257997.2:c.623_624delinsCG	NP_001244926.1:p.Pro208=