Canonical Allele Identifier: CA2215153552

Gene: IL4R

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27344914_27344921delinsGTGCCACC , CM000678.2:g.27344914_27344921delinsGTGCCACC	GRCh38
NC_000016.9:g.27356235_27356242delinsGTGCCACC , CM000678.1:g.27356235_27356242delinsGTGCCACC	GRCh37
NC_000016.8:g.27263736_27263743delinsGTGCCACC	NCBI36
NG_012086.1:g.35985_35992delinsGTGCCACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395762.7:c.255_262delinsGTGCCACC MANE Select	ENSP00000379111.2:p.Val85=
ENST00000170630.6:c.210_217delinsGTGCCACC	ENSP00000170630.3:p.Val70=
ENST00000395762.6:c.255_262delinsGTGCCACC	ENSP00000379111.2:p.Val85=
ENST00000543915.6:c.255_262delinsGTGCCACC	ENSP00000441667.2:p.Val85=
ENST00000561946.5:n.435_442delinsGTGCCACC
ENST00000562968.1:c.7_14delinsGTGCCACC
ENST00000563002.5:c.255_262delinsGTGCCACC	ENSP00000456930.1:p.Val85=
ENST00000563787.1:n.576_583delinsGTGCCACC
ENST00000565696.1:n.275_282delinsGTGCCACC
ENST00000566117.5:c.255_262delinsGTGCCACC	ENSP00000455632.1:p.Val85=
ENST00000566318.5:c.255_262delinsGTGCCACC	ENSP00000456248.1:p.Val85=
ENST00000568746.5:c.*298_*305delinsGTGCCACC	ENSP00000455714.1:n.*298_*305delinsGTGCCACC
NM_000418.3:c.255_262delinsGTGCCACC	NP_000409.1:p.Val85=
NM_001257406.1:c.255_262delinsGTGCCACC	NP_001244335.1:p.Val85=
NM_001257407.1:c.210_217delinsGTGCCACC	NP_001244336.1:p.Val70=
NM_001257997.1:c.-221_-214delinsGTGCCACC	NP_001244926.1:n.-221_-214delinsGTGCCACC
XM_011545825.1:c.255_262delinsGTGCCACC	XP_011544127.1:p.Val85=
XM_011545826.1:c.255_262delinsGTGCCACC	XP_011544128.1:p.Val85=
XM_011545827.1:c.255_262delinsGTGCCACC	XP_011544129.1:p.Val85=
XM_011545828.1:c.-13_-6delinsGTGCCACC	XP_011544130.1:n.-13_-6delinsGTGCCACC
XM_011545829.1:c.110_117delinsGTGCCACC	XP_011544131.1:p.Cys37=
XM_011545830.1:c.110_117delinsGTGCCACC	XP_011544132.1:p.Cys37=
XM_011545831.1:c.110_117delinsGTGCCACC	XP_011544133.1:p.Cys37=
XM_011545832.1:c.110_117delinsGTGCCACC	XP_011544134.1:p.Cys37=
XM_011545833.1:c.110_117delinsGTGCCACC	XP_011544135.1:p.Cys37=
XM_011545834.1:c.-17_-10delinsGTGCCACC	XP_011544136.1:n.-17_-10delinsGTGCCACC
XM_011545826.2:c.255_262delinsGTGCCACC	XP_011544128.1:p.Val85=
XM_011545827.2:c.255_262delinsGTGCCACC	XP_011544129.1:p.Val85=
XM_011545828.2:c.-13_-6delinsGTGCCACC	XP_011544130.1:n.-13_-6delinsGTGCCACC
XM_011545830.2:c.110_117delinsGTGCCACC	XP_011544132.1:p.Cys37=
XM_011545833.2:c.110_117delinsGTGCCACC	XP_011544135.1:p.Cys37=
XM_011545834.2:c.-17_-10delinsGTGCCACC	XP_011544136.1:n.-17_-10delinsGTGCCACC
XM_017023211.1:c.255_262delinsGTGCCACC	XP_016878700.1:p.Val85=
NM_000418.4:c.255_262delinsGTGCCACC MANE Select	NP_000409.1:p.Val85=
NM_001257406.2:c.255_262delinsGTGCCACC	NP_001244335.1:p.Val85=
NM_001257407.2:c.210_217delinsGTGCCACC	NP_001244336.1:p.Val70=
NM_001257997.2:c.-221_-214delinsGTGCCACC	NP_001244926.1:n.-221_-214delinsGTGCCACC