Canonical Allele Identifier: CA395298932
Gene: IL4R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.27362808G>C , CM000678.2:g.27362808G>C GRCh38
NC_000016.9:g.27374129G>C , CM000678.1:g.27374129G>C GRCh37
NC_000016.8:g.27281630G>C NCBI36
NG_012086.1:g.53879G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395762.7:c.1456G>C MANE Select ENSP00000379111.2:p.Glu486Gln
ENST00000170630.6:c.1411G>C ENSP00000170630.3:p.Glu471Gln
ENST00000395762.6:c.1456G>C ENSP00000379111.2:p.Glu486Gln
ENST00000543915.6:c.1456G>C ENSP00000441667.2:p.Glu486Gln
ENST00000565352.1:c.230-1295G>C ENSP00000461268.1:n.230-1295G>C
ENST00000568746.5:c.*1499G>C ENSP00000455714.1:n.*1499G>C
NM_000418.3:c.1456G>C NP_000409.1:p.Glu486Gln
NM_001257406.1:c.1456G>C NP_001244335.1:p.Glu486Gln
NM_001257407.1:c.1411G>C NP_001244336.1:p.Glu471Gln
NM_001257997.1:c.976G>C NP_001244926.1:p.Glu326Gln
XM_005255308.2:c.565G>C XP_005255365.1:p.Glu189Gln
XM_006721043.1:c.505G>C XP_006721106.1:p.Glu169Gln
XM_011545825.1:c.1456G>C XP_011544127.1:p.Glu486Gln
XM_011545826.1:c.1456G>C XP_011544128.1:p.Glu486Gln
XM_011545827.1:c.1456G>C XP_011544129.1:p.Glu486Gln
XM_011545828.1:c.1189G>C XP_011544130.1:p.Glu397Gln
XM_011545829.1:c.1159G>C XP_011544131.1:p.Glu387Gln
XM_011545830.1:c.1159G>C XP_011544132.1:p.Glu387Gln
XM_011545831.1:c.1159G>C XP_011544133.1:p.Glu387Gln
XM_011545832.1:c.1159G>C XP_011544134.1:p.Glu387Gln
XM_011545833.1:c.1159G>C XP_011544135.1:p.Glu387Gln
XM_011545834.1:c.1033G>C XP_011544136.1:p.Glu345Gln
XM_011545826.2:c.1456G>C XP_011544128.1:p.Glu486Gln
XM_011545827.2:c.1456G>C XP_011544129.1:p.Glu486Gln
XM_011545828.2:c.1189G>C XP_011544130.1:p.Glu397Gln
XM_011545830.2:c.1159G>C XP_011544132.1:p.Glu387Gln
XM_011545833.2:c.1159G>C XP_011544135.1:p.Glu387Gln
XM_011545834.2:c.1033G>C XP_011544136.1:p.Glu345Gln
XM_017023211.1:c.*491G>C XP_016878700.1:n.*491G>C
NM_000418.4:c.1456G>C MANE Select NP_000409.1:p.Glu486Gln
NM_001257406.2:c.1456G>C NP_001244335.1:p.Glu486Gln
NM_001257407.2:c.1411G>C NP_001244336.1:p.Glu471Gln
NM_001257997.2:c.976G>C NP_001244926.1:p.Glu326Gln