Canonical Allele Identifier: CA395297953
Gene: IL4R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.27362553G>C , CM000678.2:g.27362553G>C GRCh38
NC_000016.9:g.27373874G>C , CM000678.1:g.27373874G>C GRCh37
NC_000016.8:g.27281375G>C NCBI36
NG_012086.1:g.53624G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000395762.7:c.1201G>C MANE Select ENSP00000379111.2:p.Gly401Arg
ENST00000170630.6:c.1156G>C ENSP00000170630.3:p.Gly386Arg
ENST00000395762.6:c.1201G>C ENSP00000379111.2:p.Gly401Arg
ENST00000543915.6:c.1201G>C ENSP00000441667.2:p.Gly401Arg
ENST00000565352.1:c.230-1550G>C ENSP00000461268.1:n.230-1550G>C
ENST00000568746.5:c.*1244G>C ENSP00000455714.1:n.*1244G>C
NM_000418.3:c.1201G>C NP_000409.1:p.Gly401Arg
NM_001257406.1:c.1201G>C NP_001244335.1:p.Gly401Arg
NM_001257407.1:c.1156G>C NP_001244336.1:p.Gly386Arg
NM_001257997.1:c.721G>C NP_001244926.1:p.Gly241Arg
XM_005255308.2:c.310G>C XP_005255365.1:p.Gly104Arg
XM_006721043.1:c.250G>C XP_006721106.1:p.Gly84Arg
XM_011545825.1:c.1201G>C XP_011544127.1:p.Gly401Arg
XM_011545826.1:c.1201G>C XP_011544128.1:p.Gly401Arg
XM_011545827.1:c.1201G>C XP_011544129.1:p.Gly401Arg
XM_011545828.1:c.934G>C XP_011544130.1:p.Gly312Arg
XM_011545829.1:c.904G>C XP_011544131.1:p.Gly302Arg
XM_011545830.1:c.904G>C XP_011544132.1:p.Gly302Arg
XM_011545831.1:c.904G>C XP_011544133.1:p.Gly302Arg
XM_011545832.1:c.904G>C XP_011544134.1:p.Gly302Arg
XM_011545833.1:c.904G>C XP_011544135.1:p.Gly302Arg
XM_011545834.1:c.778G>C XP_011544136.1:p.Gly260Arg
XM_011545826.2:c.1201G>C XP_011544128.1:p.Gly401Arg
XM_011545827.2:c.1201G>C XP_011544129.1:p.Gly401Arg
XM_011545828.2:c.934G>C XP_011544130.1:p.Gly312Arg
XM_011545830.2:c.904G>C XP_011544132.1:p.Gly302Arg
XM_011545833.2:c.904G>C XP_011544135.1:p.Gly302Arg
XM_011545834.2:c.778G>C XP_011544136.1:p.Gly260Arg
XM_017023211.1:c.*236G>C XP_016878700.1:n.*236G>C
NM_000418.4:c.1201G>C MANE Select NP_000409.1:p.Gly401Arg
NM_001257406.2:c.1201G>C NP_001244335.1:p.Gly401Arg
NM_001257407.2:c.1156G>C NP_001244336.1:p.Gly386Arg
NM_001257997.2:c.721G>C NP_001244926.1:p.Gly241Arg