Canonical Allele Identifier: CA395298929

Gene: IL4R

Linked Data

• gnomAD v4: 16-27362806-C-G
• MyVariant Identifiers: chr16:g.27374127C>G (hg19) ; chr16:g.27362806C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27362806C>G , CM000678.2:g.27362806C>G	GRCh38
NC_000016.9:g.27374127C>G , CM000678.1:g.27374127C>G	GRCh37
NC_000016.8:g.27281628C>G	NCBI36
NG_012086.1:g.53877C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395762.7:c.1454C>G MANE Select	ENSP00000379111.2:p.Thr485Arg
ENST00000170630.6:c.1409C>G	ENSP00000170630.3:p.Thr470Arg
ENST00000395762.6:c.1454C>G	ENSP00000379111.2:p.Thr485Arg
ENST00000543915.6:c.1454C>G	ENSP00000441667.2:p.Thr485Arg
ENST00000565352.1:c.230-1297C>G	ENSP00000461268.1:n.230-1297C>G
ENST00000568746.5:c.*1497C>G	ENSP00000455714.1:n.*1497C>G
NM_000418.3:c.1454C>G	NP_000409.1:p.Thr485Arg
NM_001257406.1:c.1454C>G	NP_001244335.1:p.Thr485Arg
NM_001257407.1:c.1409C>G	NP_001244336.1:p.Thr470Arg
NM_001257997.1:c.974C>G	NP_001244926.1:p.Thr325Arg
XM_005255308.2:c.563C>G	XP_005255365.1:p.Thr188Arg
XM_006721043.1:c.503C>G	XP_006721106.1:p.Thr168Arg
XM_011545825.1:c.1454C>G	XP_011544127.1:p.Thr485Arg
XM_011545826.1:c.1454C>G	XP_011544128.1:p.Thr485Arg
XM_011545827.1:c.1454C>G	XP_011544129.1:p.Thr485Arg
XM_011545828.1:c.1187C>G	XP_011544130.1:p.Thr396Arg
XM_011545829.1:c.1157C>G	XP_011544131.1:p.Thr386Arg
XM_011545830.1:c.1157C>G	XP_011544132.1:p.Thr386Arg
XM_011545831.1:c.1157C>G	XP_011544133.1:p.Thr386Arg
XM_011545832.1:c.1157C>G	XP_011544134.1:p.Thr386Arg
XM_011545833.1:c.1157C>G	XP_011544135.1:p.Thr386Arg
XM_011545834.1:c.1031C>G	XP_011544136.1:p.Thr344Arg
XM_011545826.2:c.1454C>G	XP_011544128.1:p.Thr485Arg
XM_011545827.2:c.1454C>G	XP_011544129.1:p.Thr485Arg
XM_011545828.2:c.1187C>G	XP_011544130.1:p.Thr396Arg
XM_011545830.2:c.1157C>G	XP_011544132.1:p.Thr386Arg
XM_011545833.2:c.1157C>G	XP_011544135.1:p.Thr386Arg
XM_011545834.2:c.1031C>G	XP_011544136.1:p.Thr344Arg
XM_017023211.1:c.*489C>G	XP_016878700.1:n.*489C>G
NM_000418.4:c.1454C>G MANE Select	NP_000409.1:p.Thr485Arg
NM_001257406.2:c.1454C>G	NP_001244335.1:p.Thr485Arg
NM_001257407.2:c.1409C>G	NP_001244336.1:p.Thr470Arg
NM_001257997.2:c.974C>G	NP_001244926.1:p.Thr325Arg