Canonical Allele Identifier: CA395305500
Gene: IL4R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.27344883T>A , CM000678.2:g.27344883T>A GRCh38
NC_000016.9:g.27356204T>A , CM000678.1:g.27356204T>A GRCh37
NC_000016.8:g.27263705T>A NCBI36
NG_012086.1:g.35954T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395762.7:c.224T>A MANE Select ENSP00000379111.2:p.Ile75Asn
ENST00000170630.6:c.179T>A ENSP00000170630.3:p.Ile60Asn
ENST00000395762.6:c.224T>A ENSP00000379111.2:p.Ile75Asn
ENST00000543915.6:c.224T>A ENSP00000441667.2:p.Ile75Asn
ENST00000561946.5:n.404T>A
ENST00000563002.5:c.224T>A ENSP00000456930.1:p.Ile75Asn
ENST00000563787.1:n.545T>A
ENST00000565696.1:n.244T>A
ENST00000566117.5:c.224T>A ENSP00000455632.1:p.Ile75Asn
ENST00000566318.5:c.224T>A ENSP00000456248.1:p.Ile75Asn
ENST00000568746.5:c.*267T>A ENSP00000455714.1:n.*267T>A
NM_000418.3:c.224T>A NP_000409.1:p.Ile75Asn
NM_001257406.1:c.224T>A NP_001244335.1:p.Ile75Asn
NM_001257407.1:c.179T>A NP_001244336.1:p.Ile60Asn
NM_001257997.1:c.-252T>A NP_001244926.1:n.-252T>A
XM_011545825.1:c.224T>A XP_011544127.1:p.Ile75Asn
XM_011545826.1:c.224T>A XP_011544128.1:p.Ile75Asn
XM_011545827.1:c.224T>A XP_011544129.1:p.Ile75Asn
XM_011545828.1:c.-44T>A XP_011544130.1:n.-44T>A
XM_011545829.1:c.79T>A XP_011544131.1:p.Ser27Thr
XM_011545830.1:c.79T>A XP_011544132.1:p.Ser27Thr
XM_011545831.1:c.79T>A XP_011544133.1:p.Ser27Thr
XM_011545832.1:c.79T>A XP_011544134.1:p.Ser27Thr
XM_011545833.1:c.79T>A XP_011544135.1:p.Ser27Thr
XM_011545834.1:c.-48T>A XP_011544136.1:n.-48T>A
XM_011545826.2:c.224T>A XP_011544128.1:p.Ile75Asn
XM_011545827.2:c.224T>A XP_011544129.1:p.Ile75Asn
XM_011545828.2:c.-44T>A XP_011544130.1:n.-44T>A
XM_011545830.2:c.79T>A XP_011544132.1:p.Ser27Thr
XM_011545833.2:c.79T>A XP_011544135.1:p.Ser27Thr
XM_011545834.2:c.-48T>A XP_011544136.1:n.-48T>A
XM_017023211.1:c.224T>A XP_016878700.1:p.Ile75Asn
NM_000418.4:c.224T>A MANE Select NP_000409.1:p.Ile75Asn
NM_001257406.2:c.224T>A NP_001244335.1:p.Ile75Asn
NM_001257407.2:c.179T>A NP_001244336.1:p.Ile60Asn
NM_001257997.2:c.-252T>A NP_001244926.1:n.-252T>A