Canonical Allele Identifier: CA494470171

Gene: IL4R

Linked Data

• MyVariant Identifiers: chr16:g.27374179C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27362858C>T , CM000678.2:g.27362858C>T	GRCh38
NC_000016.9:g.27374179C>T , CM000678.1:g.27374179C>T	GRCh37
NC_000016.8:g.27281680C>T	NCBI36
NG_012086.1:g.53929C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395762.7:c.1506C>T MANE Select	ENSP00000379111.2:p.Asn502=
ENST00000170630.6:c.1461C>T	ENSP00000170630.3:p.Asn487=
ENST00000395762.6:c.1506C>T	ENSP00000379111.2:p.Asn502=
ENST00000543915.6:c.1506C>T	ENSP00000441667.2:p.Asn502=
ENST00000565352.1:c.230-1245C>T	ENSP00000461268.1:n.230-1245C>T
ENST00000568746.5:c.*1549C>T	ENSP00000455714.1:n.*1549C>T
NM_000418.3:c.1506C>T	NP_000409.1:p.Asn502=
NM_001257406.1:c.1506C>T	NP_001244335.1:p.Asn502=
NM_001257407.1:c.1461C>T	NP_001244336.1:p.Asn487=
NM_001257997.1:c.1026C>T	NP_001244926.1:p.Asn342=
XM_005255308.2:c.615C>T	XP_005255365.1:p.Asn205=
XM_006721043.1:c.555C>T	XP_006721106.1:p.Asn185=
XM_011545825.1:c.1506C>T	XP_011544127.1:p.Asn502=
XM_011545826.1:c.1506C>T	XP_011544128.1:p.Asn502=
XM_011545827.1:c.1506C>T	XP_011544129.1:p.Asn502=
XM_011545828.1:c.1239C>T	XP_011544130.1:p.Asn413=
XM_011545829.1:c.1209C>T	XP_011544131.1:p.Asn403=
XM_011545830.1:c.1209C>T	XP_011544132.1:p.Asn403=
XM_011545831.1:c.1209C>T	XP_011544133.1:p.Asn403=
XM_011545832.1:c.1209C>T	XP_011544134.1:p.Asn403=
XM_011545833.1:c.1209C>T	XP_011544135.1:p.Asn403=
XM_011545834.1:c.1083C>T	XP_011544136.1:p.Asn361=
XM_011545826.2:c.1506C>T	XP_011544128.1:p.Asn502=
XM_011545827.2:c.1506C>T	XP_011544129.1:p.Asn502=
XM_011545828.2:c.1239C>T	XP_011544130.1:p.Asn413=
XM_011545830.2:c.1209C>T	XP_011544132.1:p.Asn403=
XM_011545833.2:c.1209C>T	XP_011544135.1:p.Asn403=
XM_011545834.2:c.1083C>T	XP_011544136.1:p.Asn361=
NM_000418.4:c.1506C>T MANE Select	NP_000409.1:p.Asn502=
NM_001257406.2:c.1506C>T	NP_001244335.1:p.Asn502=
NM_001257407.2:c.1461C>T	NP_001244336.1:p.Asn487=
NM_001257997.2:c.1026C>T	NP_001244926.1:p.Asn342=