Canonical Allele Identifier: CA395298633
Gene: IL4R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.27362693G>T , CM000678.2:g.27362693G>T GRCh38
NC_000016.9:g.27374014G>T , CM000678.1:g.27374014G>T GRCh37
NC_000016.8:g.27281515G>T NCBI36
NG_012086.1:g.53764G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395762.7:c.1341G>T MANE Select ENSP00000379111.2:p.Glu447Asp
ENST00000170630.6:c.1296G>T ENSP00000170630.3:p.Glu432Asp
ENST00000395762.6:c.1341G>T ENSP00000379111.2:p.Glu447Asp
ENST00000543915.6:c.1341G>T ENSP00000441667.2:p.Glu447Asp
ENST00000565352.1:c.230-1410G>T ENSP00000461268.1:n.230-1410G>T
ENST00000568746.5:c.*1384G>T ENSP00000455714.1:n.*1384G>T
NM_000418.3:c.1341G>T NP_000409.1:p.Glu447Asp
NM_001257406.1:c.1341G>T NP_001244335.1:p.Glu447Asp
NM_001257407.1:c.1296G>T NP_001244336.1:p.Glu432Asp
NM_001257997.1:c.861G>T NP_001244926.1:p.Glu287Asp
XM_005255308.2:c.450G>T XP_005255365.1:p.Glu150Asp
XM_006721043.1:c.390G>T XP_006721106.1:p.Glu130Asp
XM_011545825.1:c.1341G>T XP_011544127.1:p.Glu447Asp
XM_011545826.1:c.1341G>T XP_011544128.1:p.Glu447Asp
XM_011545827.1:c.1341G>T XP_011544129.1:p.Glu447Asp
XM_011545828.1:c.1074G>T XP_011544130.1:p.Glu358Asp
XM_011545829.1:c.1044G>T XP_011544131.1:p.Glu348Asp
XM_011545830.1:c.1044G>T XP_011544132.1:p.Glu348Asp
XM_011545831.1:c.1044G>T XP_011544133.1:p.Glu348Asp
XM_011545832.1:c.1044G>T XP_011544134.1:p.Glu348Asp
XM_011545833.1:c.1044G>T XP_011544135.1:p.Glu348Asp
XM_011545834.1:c.918G>T XP_011544136.1:p.Glu306Asp
XM_011545826.2:c.1341G>T XP_011544128.1:p.Glu447Asp
XM_011545827.2:c.1341G>T XP_011544129.1:p.Glu447Asp
XM_011545828.2:c.1074G>T XP_011544130.1:p.Glu358Asp
XM_011545830.2:c.1044G>T XP_011544132.1:p.Glu348Asp
XM_011545833.2:c.1044G>T XP_011544135.1:p.Glu348Asp
XM_011545834.2:c.918G>T XP_011544136.1:p.Glu306Asp
XM_017023211.1:c.*376G>T XP_016878700.1:n.*376G>T
NM_000418.4:c.1341G>T MANE Select NP_000409.1:p.Glu447Asp
NM_001257406.2:c.1341G>T NP_001244335.1:p.Glu447Asp
NM_001257407.2:c.1296G>T NP_001244336.1:p.Glu432Asp
NM_001257997.2:c.861G>T NP_001244926.1:p.Glu287Asp