Canonical Allele Identifier: CA395298683

Gene: IL4R

Linked Data

• MyVariant Identifiers: chr16:g.27374024G>A (hg19) ; chr16:g.27362703G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27362703G>A , CM000678.2:g.27362703G>A	GRCh38
NC_000016.9:g.27374024G>A , CM000678.1:g.27374024G>A	GRCh37
NC_000016.8:g.27281525G>A	NCBI36
NG_012086.1:g.53774G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395762.7:c.1351G>A MANE Select	ENSP00000379111.2:p.Ala451Thr
ENST00000170630.6:c.1306G>A	ENSP00000170630.3:p.Ala436Thr
ENST00000395762.6:c.1351G>A	ENSP00000379111.2:p.Ala451Thr
ENST00000543915.6:c.1351G>A	ENSP00000441667.2:p.Ala451Thr
ENST00000565352.1:c.230-1400G>A	ENSP00000461268.1:n.230-1400G>A
ENST00000568746.5:c.*1394G>A	ENSP00000455714.1:n.*1394G>A
NM_000418.3:c.1351G>A	NP_000409.1:p.Ala451Thr
NM_001257406.1:c.1351G>A	NP_001244335.1:p.Ala451Thr
NM_001257407.1:c.1306G>A	NP_001244336.1:p.Ala436Thr
NM_001257997.1:c.871G>A	NP_001244926.1:p.Ala291Thr
XM_005255308.2:c.460G>A	XP_005255365.1:p.Ala154Thr
XM_006721043.1:c.400G>A	XP_006721106.1:p.Ala134Thr
XM_011545825.1:c.1351G>A	XP_011544127.1:p.Ala451Thr
XM_011545826.1:c.1351G>A	XP_011544128.1:p.Ala451Thr
XM_011545827.1:c.1351G>A	XP_011544129.1:p.Ala451Thr
XM_011545828.1:c.1084G>A	XP_011544130.1:p.Ala362Thr
XM_011545829.1:c.1054G>A	XP_011544131.1:p.Ala352Thr
XM_011545830.1:c.1054G>A	XP_011544132.1:p.Ala352Thr
XM_011545831.1:c.1054G>A	XP_011544133.1:p.Ala352Thr
XM_011545832.1:c.1054G>A	XP_011544134.1:p.Ala352Thr
XM_011545833.1:c.1054G>A	XP_011544135.1:p.Ala352Thr
XM_011545834.1:c.928G>A	XP_011544136.1:p.Ala310Thr
XM_011545826.2:c.1351G>A	XP_011544128.1:p.Ala451Thr
XM_011545827.2:c.1351G>A	XP_011544129.1:p.Ala451Thr
XM_011545828.2:c.1084G>A	XP_011544130.1:p.Ala362Thr
XM_011545830.2:c.1054G>A	XP_011544132.1:p.Ala352Thr
XM_011545833.2:c.1054G>A	XP_011544135.1:p.Ala352Thr
XM_011545834.2:c.928G>A	XP_011544136.1:p.Ala310Thr
XM_017023211.1:c.*386G>A	XP_016878700.1:n.*386G>A
NM_000418.4:c.1351G>A MANE Select	NP_000409.1:p.Ala451Thr
NM_001257406.2:c.1351G>A	NP_001244335.1:p.Ala451Thr
NM_001257407.2:c.1306G>A	NP_001244336.1:p.Ala436Thr
NM_001257997.2:c.871G>A	NP_001244926.1:p.Ala291Thr