Canonical Allele Identifier: CA395298192
Gene: IL4R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.27362611G>C , CM000678.2:g.27362611G>C GRCh38
NC_000016.9:g.27373932G>C , CM000678.1:g.27373932G>C GRCh37
NC_000016.8:g.27281433G>C NCBI36
NG_012086.1:g.53682G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395762.7:c.1259G>C MANE Select ENSP00000379111.2:p.Gly420Ala
ENST00000170630.6:c.1214G>C ENSP00000170630.3:p.Gly405Ala
ENST00000395762.6:c.1259G>C ENSP00000379111.2:p.Gly420Ala
ENST00000543915.6:c.1259G>C ENSP00000441667.2:p.Gly420Ala
ENST00000565352.1:c.230-1492G>C ENSP00000461268.1:n.230-1492G>C
ENST00000568746.5:c.*1302G>C ENSP00000455714.1:n.*1302G>C
NM_000418.3:c.1259G>C NP_000409.1:p.Gly420Ala
NM_001257406.1:c.1259G>C NP_001244335.1:p.Gly420Ala
NM_001257407.1:c.1214G>C NP_001244336.1:p.Gly405Ala
NM_001257997.1:c.779G>C NP_001244926.1:p.Gly260Ala
XM_005255308.2:c.368G>C XP_005255365.1:p.Gly123Ala
XM_006721043.1:c.308G>C XP_006721106.1:p.Gly103Ala
XM_011545825.1:c.1259G>C XP_011544127.1:p.Gly420Ala
XM_011545826.1:c.1259G>C XP_011544128.1:p.Gly420Ala
XM_011545827.1:c.1259G>C XP_011544129.1:p.Gly420Ala
XM_011545828.1:c.992G>C XP_011544130.1:p.Gly331Ala
XM_011545829.1:c.962G>C XP_011544131.1:p.Gly321Ala
XM_011545830.1:c.962G>C XP_011544132.1:p.Gly321Ala
XM_011545831.1:c.962G>C XP_011544133.1:p.Gly321Ala
XM_011545832.1:c.962G>C XP_011544134.1:p.Gly321Ala
XM_011545833.1:c.962G>C XP_011544135.1:p.Gly321Ala
XM_011545834.1:c.836G>C XP_011544136.1:p.Gly279Ala
XM_011545826.2:c.1259G>C XP_011544128.1:p.Gly420Ala
XM_011545827.2:c.1259G>C XP_011544129.1:p.Gly420Ala
XM_011545828.2:c.992G>C XP_011544130.1:p.Gly331Ala
XM_011545830.2:c.962G>C XP_011544132.1:p.Gly321Ala
XM_011545833.2:c.962G>C XP_011544135.1:p.Gly321Ala
XM_011545834.2:c.836G>C XP_011544136.1:p.Gly279Ala
XM_017023211.1:c.*294G>C XP_016878700.1:n.*294G>C
NM_000418.4:c.1259G>C MANE Select NP_000409.1:p.Gly420Ala
NM_001257406.2:c.1259G>C NP_001244335.1:p.Gly420Ala
NM_001257407.2:c.1214G>C NP_001244336.1:p.Gly405Ala
NM_001257997.2:c.779G>C NP_001244926.1:p.Gly260Ala