Canonical Allele Identifier: CA2215169765

Gene: IL4R

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27362774C= , CM000678.2:g.27362774C=	GRCh38
NC_000016.9:g.27374095C= , CM000678.1:g.27374095C=	GRCh37
NC_000016.8:g.27281596C=	NCBI36
NG_012086.1:g.53845C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395762.7:c.1422C= MANE Select	ENSP00000379111.2:p.Ser474=
ENST00000170630.6:c.1377C=	ENSP00000170630.3:p.Ser459=
ENST00000395762.6:c.1422C=	ENSP00000379111.2:p.Ser474=
ENST00000543915.6:c.1422C=	ENSP00000441667.2:p.Ser474=
ENST00000565352.1:c.230-1329C=	ENSP00000461268.1:n.230-1329C=
ENST00000568746.5:c.*1465C=	ENSP00000455714.1:n.*1465C=
NM_000418.3:c.1422C=	NP_000409.1:p.Ser474=
NM_001257406.1:c.1422C=	NP_001244335.1:p.Ser474=
NM_001257407.1:c.1377C=	NP_001244336.1:p.Ser459=
NM_001257997.1:c.942C=	NP_001244926.1:p.Ser314=
XM_005255308.2:c.531C=	XP_005255365.1:p.Ser177=
XM_006721043.1:c.471C=	XP_006721106.1:p.Ser157=
XM_011545825.1:c.1422C=	XP_011544127.1:p.Ser474=
XM_011545826.1:c.1422C=	XP_011544128.1:p.Ser474=
XM_011545827.1:c.1422C=	XP_011544129.1:p.Ser474=
XM_011545828.1:c.1155C=	XP_011544130.1:p.Ser385=
XM_011545829.1:c.1125C=	XP_011544131.1:p.Ser375=
XM_011545830.1:c.1125C=	XP_011544132.1:p.Ser375=
XM_011545831.1:c.1125C=	XP_011544133.1:p.Ser375=
XM_011545832.1:c.1125C=	XP_011544134.1:p.Ser375=
XM_011545833.1:c.1125C=	XP_011544135.1:p.Ser375=
XM_011545834.1:c.999C=	XP_011544136.1:p.Ser333=
XM_011545826.2:c.1422C=	XP_011544128.1:p.Ser474=
XM_011545827.2:c.1422C=	XP_011544129.1:p.Ser474=
XM_011545828.2:c.1155C=	XP_011544130.1:p.Ser385=
XM_011545830.2:c.1125C=	XP_011544132.1:p.Ser375=
XM_011545833.2:c.1125C=	XP_011544135.1:p.Ser375=
XM_011545834.2:c.999C=	XP_011544136.1:p.Ser333=
XM_017023211.1:c.*457C=	XP_016878700.1:n.*457C=
NM_000418.4:c.1422C= MANE Select	NP_000409.1:p.Ser474=
NM_001257406.2:c.1422C=	NP_001244335.1:p.Ser474=
NM_001257407.2:c.1377C=	NP_001244336.1:p.Ser459=
NM_001257997.2:c.942C=	NP_001244926.1:p.Ser314=