Canonical Allele Identifier: CA2215153564

Gene: IL4R

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27344924C= , CM000678.2:g.27344924C=	GRCh38
NC_000016.9:g.27356245C= , CM000678.1:g.27356245C=	GRCh37
NC_000016.8:g.27263746C=	NCBI36
NG_012086.1:g.35995C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395762.7:c.265C= MANE Select	ENSP00000379111.2:p.Leu89=
ENST00000170630.6:c.220C=	ENSP00000170630.3:p.Leu74=
ENST00000395762.6:c.265C=	ENSP00000379111.2:p.Leu89=
ENST00000543915.6:c.265C=	ENSP00000441667.2:p.Leu89=
ENST00000561946.5:n.445C=
ENST00000562968.1:c.17C=
ENST00000563002.5:c.265C=	ENSP00000456930.1:p.Leu89=
ENST00000563787.1:n.586C=
ENST00000565696.1:n.285C=
ENST00000566117.5:c.265C=	ENSP00000455632.1:p.Leu89=
ENST00000566318.5:c.265C=	ENSP00000456248.1:p.Leu89=
ENST00000568746.5:c.*308C=	ENSP00000455714.1:n.*308C=
NM_000418.3:c.265C=	NP_000409.1:p.Leu89=
NM_001257406.1:c.265C=	NP_001244335.1:p.Leu89=
NM_001257407.1:c.220C=	NP_001244336.1:p.Leu74=
NM_001257997.1:c.-211C=	NP_001244926.1:n.-211C=
XM_011545825.1:c.265C=	XP_011544127.1:p.Leu89=
XM_011545826.1:c.265C=	XP_011544128.1:p.Leu89=
XM_011545827.1:c.265C=	XP_011544129.1:p.Leu89=
XM_011545828.1:c.-3C=	XP_011544130.1:n.-3C=
XM_011545829.1:c.120C=	XP_011544131.1:p.Cys40=
XM_011545830.1:c.120C=	XP_011544132.1:p.Cys40=
XM_011545831.1:c.120C=	XP_011544133.1:p.Cys40=
XM_011545832.1:c.120C=	XP_011544134.1:p.Cys40=
XM_011545833.1:c.120C=	XP_011544135.1:p.Cys40=
XM_011545834.1:c.-7C=	XP_011544136.1:n.-7C=
XM_011545826.2:c.265C=	XP_011544128.1:p.Leu89=
XM_011545827.2:c.265C=	XP_011544129.1:p.Leu89=
XM_011545828.2:c.-3C=	XP_011544130.1:n.-3C=
XM_011545830.2:c.120C=	XP_011544132.1:p.Cys40=
XM_011545833.2:c.120C=	XP_011544135.1:p.Cys40=
XM_011545834.2:c.-7C=	XP_011544136.1:n.-7C=
XM_017023211.1:c.265C=	XP_016878700.1:p.Leu89=
NM_000418.4:c.265C= MANE Select	NP_000409.1:p.Leu89=
NM_001257406.2:c.265C=	NP_001244335.1:p.Leu89=
NM_001257407.2:c.220C=	NP_001244336.1:p.Leu74=
NM_001257997.2:c.-211C=	NP_001244926.1:n.-211C=