Canonical Allele Identifier: CA395297626
Gene: IL4R HGNC NCBI

Linked Data

dbSNP Id: rs141632606

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.27362452C>G , CM000678.2:g.27362452C>G GRCh38
NC_000016.9:g.27373773C>G , CM000678.1:g.27373773C>G GRCh37
NC_000016.8:g.27281274C>G NCBI36
NG_012086.1:g.53523C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395762.7:c.1100C>G MANE Select ENSP00000379111.2:p.Ala367Gly
ENST00000170630.6:c.1055C>G ENSP00000170630.3:p.Ala352Gly
ENST00000395762.6:c.1100C>G ENSP00000379111.2:p.Ala367Gly
ENST00000543915.6:c.1100C>G ENSP00000441667.2:p.Ala367Gly
ENST00000565352.1:c.230-1651C>G ENSP00000461268.1:n.230-1651C>G
ENST00000565915.5:n.510C>G
ENST00000568746.5:c.*1143C>G ENSP00000455714.1:n.*1143C>G
NM_000418.3:c.1100C>G NP_000409.1:p.Ala367Gly
NM_001257406.1:c.1100C>G NP_001244335.1:p.Ala367Gly
NM_001257407.1:c.1055C>G NP_001244336.1:p.Ala352Gly
NM_001257997.1:c.620C>G NP_001244926.1:p.Ala207Gly
XM_005255308.2:c.209C>G XP_005255365.1:p.Ala70Gly
XM_006721043.1:c.149C>G XP_006721106.1:p.Ala50Gly
XM_011545825.1:c.1100C>G XP_011544127.1:p.Ala367Gly
XM_011545826.1:c.1100C>G XP_011544128.1:p.Ala367Gly
XM_011545827.1:c.1100C>G XP_011544129.1:p.Ala367Gly
XM_011545828.1:c.833C>G XP_011544130.1:p.Ala278Gly
XM_011545829.1:c.803C>G XP_011544131.1:p.Ala268Gly
XM_011545830.1:c.803C>G XP_011544132.1:p.Ala268Gly
XM_011545831.1:c.803C>G XP_011544133.1:p.Ala268Gly
XM_011545832.1:c.803C>G XP_011544134.1:p.Ala268Gly
XM_011545833.1:c.803C>G XP_011544135.1:p.Ala268Gly
XM_011545834.1:c.677C>G XP_011544136.1:p.Ala226Gly
XM_011545826.2:c.1100C>G XP_011544128.1:p.Ala367Gly
XM_011545827.2:c.1100C>G XP_011544129.1:p.Ala367Gly
XM_011545828.2:c.833C>G XP_011544130.1:p.Ala278Gly
XM_011545830.2:c.803C>G XP_011544132.1:p.Ala268Gly
XM_011545833.2:c.803C>G XP_011544135.1:p.Ala268Gly
XM_011545834.2:c.677C>G XP_011544136.1:p.Ala226Gly
XM_017023211.1:c.*135C>G XP_016878700.1:n.*135C>G
NM_000418.4:c.1100C>G MANE Select NP_000409.1:p.Ala367Gly
NM_001257406.2:c.1100C>G NP_001244335.1:p.Ala367Gly
NM_001257407.2:c.1055C>G NP_001244336.1:p.Ala352Gly
NM_001257997.2:c.620C>G NP_001244926.1:p.Ala207Gly