Canonical Allele Identifier: CA395298961
Gene: IL4R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.27362823A>G , CM000678.2:g.27362823A>G GRCh38
NC_000016.9:g.27374144A>G , CM000678.1:g.27374144A>G GRCh37
NC_000016.8:g.27281645A>G NCBI36
NG_012086.1:g.53894A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395762.7:c.1471A>G MANE Select ENSP00000379111.2:p.Ile491Val
ENST00000170630.6:c.1426A>G ENSP00000170630.3:p.Ile476Val
ENST00000395762.6:c.1471A>G ENSP00000379111.2:p.Ile491Val
ENST00000543915.6:c.1471A>G ENSP00000441667.2:p.Ile491Val
ENST00000565352.1:c.230-1280A>G ENSP00000461268.1:n.230-1280A>G
ENST00000568746.5:c.*1514A>G ENSP00000455714.1:n.*1514A>G
NM_000418.3:c.1471A>G NP_000409.1:p.Ile491Val
NM_001257406.1:c.1471A>G NP_001244335.1:p.Ile491Val
NM_001257407.1:c.1426A>G NP_001244336.1:p.Ile476Val
NM_001257997.1:c.991A>G NP_001244926.1:p.Ile331Val
XM_005255308.2:c.580A>G XP_005255365.1:p.Ile194Val
XM_006721043.1:c.520A>G XP_006721106.1:p.Ile174Val
XM_011545825.1:c.1471A>G XP_011544127.1:p.Ile491Val
XM_011545826.1:c.1471A>G XP_011544128.1:p.Ile491Val
XM_011545827.1:c.1471A>G XP_011544129.1:p.Ile491Val
XM_011545828.1:c.1204A>G XP_011544130.1:p.Ile402Val
XM_011545829.1:c.1174A>G XP_011544131.1:p.Ile392Val
XM_011545830.1:c.1174A>G XP_011544132.1:p.Ile392Val
XM_011545831.1:c.1174A>G XP_011544133.1:p.Ile392Val
XM_011545832.1:c.1174A>G XP_011544134.1:p.Ile392Val
XM_011545833.1:c.1174A>G XP_011544135.1:p.Ile392Val
XM_011545834.1:c.1048A>G XP_011544136.1:p.Ile350Val
XM_011545826.2:c.1471A>G XP_011544128.1:p.Ile491Val
XM_011545827.2:c.1471A>G XP_011544129.1:p.Ile491Val
XM_011545828.2:c.1204A>G XP_011544130.1:p.Ile402Val
XM_011545830.2:c.1174A>G XP_011544132.1:p.Ile392Val
XM_011545833.2:c.1174A>G XP_011544135.1:p.Ile392Val
XM_011545834.2:c.1048A>G XP_011544136.1:p.Ile350Val
XM_017023211.1:c.*506A>G XP_016878700.1:n.*506A>G
NM_000418.4:c.1471A>G MANE Select NP_000409.1:p.Ile491Val
NM_001257406.2:c.1471A>G NP_001244335.1:p.Ile491Val
NM_001257407.2:c.1426A>G NP_001244336.1:p.Ile476Val
NM_001257997.2:c.991A>G NP_001244926.1:p.Ile331Val