Canonical Allele Identifier: CA2215169605

Gene: IL4R

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27362663A= , CM000678.2:g.27362663A=	GRCh38
NC_000016.9:g.27373984A= , CM000678.1:g.27373984A=	GRCh37
NC_000016.8:g.27281485A=	NCBI36
NG_012086.1:g.53734A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395762.7:c.1311A= MANE Select	ENSP00000379111.2:p.Gly437=
ENST00000170630.6:c.1266A=	ENSP00000170630.3:p.Gly422=
ENST00000395762.6:c.1311A=	ENSP00000379111.2:p.Gly437=
ENST00000543915.6:c.1311A=	ENSP00000441667.2:p.Gly437=
ENST00000565352.1:c.230-1440A=	ENSP00000461268.1:n.230-1440A=
ENST00000568746.5:c.*1354A=	ENSP00000455714.1:n.*1354A=
NM_000418.3:c.1311A=	NP_000409.1:p.Gly437=
NM_001257406.1:c.1311A=	NP_001244335.1:p.Gly437=
NM_001257407.1:c.1266A=	NP_001244336.1:p.Gly422=
NM_001257997.1:c.831A=	NP_001244926.1:p.Gly277=
XM_005255308.2:c.420A=	XP_005255365.1:p.Gly140=
XM_006721043.1:c.360A=	XP_006721106.1:p.Gly120=
XM_011545825.1:c.1311A=	XP_011544127.1:p.Gly437=
XM_011545826.1:c.1311A=	XP_011544128.1:p.Gly437=
XM_011545827.1:c.1311A=	XP_011544129.1:p.Gly437=
XM_011545828.1:c.1044A=	XP_011544130.1:p.Gly348=
XM_011545829.1:c.1014A=	XP_011544131.1:p.Gly338=
XM_011545830.1:c.1014A=	XP_011544132.1:p.Gly338=
XM_011545831.1:c.1014A=	XP_011544133.1:p.Gly338=
XM_011545832.1:c.1014A=	XP_011544134.1:p.Gly338=
XM_011545833.1:c.1014A=	XP_011544135.1:p.Gly338=
XM_011545834.1:c.888A=	XP_011544136.1:p.Gly296=
XM_011545826.2:c.1311A=	XP_011544128.1:p.Gly437=
XM_011545827.2:c.1311A=	XP_011544129.1:p.Gly437=
XM_011545828.2:c.1044A=	XP_011544130.1:p.Gly348=
XM_011545830.2:c.1014A=	XP_011544132.1:p.Gly338=
XM_011545833.2:c.1014A=	XP_011544135.1:p.Gly338=
XM_011545834.2:c.888A=	XP_011544136.1:p.Gly296=
XM_017023211.1:c.*346A=	XP_016878700.1:n.*346A=
NM_000418.4:c.1311A= MANE Select	NP_000409.1:p.Gly437=
NM_001257406.2:c.1311A=	NP_001244335.1:p.Gly437=
NM_001257407.2:c.1266A=	NP_001244336.1:p.Gly422=
NM_001257997.2:c.831A=	NP_001244926.1:p.Gly277=