Canonical Allele Identifier: CA395308471

Gene: IL4R

Linked Data

• MyVariant Identifiers: chr16:g.27357931C>G (hg19) ; chr16:g.27346610C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27346610C>G , CM000678.2:g.27346610C>G	GRCh38
NC_000016.9:g.27357931C>G , CM000678.1:g.27357931C>G	GRCh37
NC_000016.8:g.27265432C>G	NCBI36
NG_012086.1:g.37681C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000395762.7:c.505C>G MANE Select	ENSP00000379111.2:p.Pro169Ala
ENST00000170630.6:c.460C>G	ENSP00000170630.3:p.Pro154Ala
ENST00000395762.6:c.505C>G	ENSP00000379111.2:p.Pro169Ala
ENST00000543915.6:c.505C>G	ENSP00000441667.2:p.Pro169Ala
ENST00000565696.1:n.525C>G
ENST00000566318.5:c.361+1590C>G	ENSP00000456248.1:n.361+1590C>G
ENST00000568746.5:c.*548C>G	ENSP00000455714.1:n.*548C>G
NM_000418.3:c.505C>G	NP_000409.1:p.Pro169Ala
NM_001257406.1:c.505C>G	NP_001244335.1:p.Pro169Ala
NM_001257407.1:c.460C>G	NP_001244336.1:p.Pro154Ala
NM_001257997.1:c.30C>G	NP_001244926.1:p.Thr10=
XM_011545825.1:c.505C>G	XP_011544127.1:p.Pro169Ala
XM_011545826.1:c.505C>G	XP_011544128.1:p.Pro169Ala
XM_011545827.1:c.505C>G	XP_011544129.1:p.Pro169Ala
XM_011545828.1:c.238C>G	XP_011544130.1:p.Pro80Ala
XM_011545829.1:c.216+1590C>G	XP_011544131.1:n.216+1590C>G
XM_011545830.1:c.216+1590C>G	XP_011544132.1:n.216+1590C>G
XM_011545831.1:c.216+1590C>G	XP_011544133.1:n.216+1590C>G
XM_011545832.1:c.216+1590C>G	XP_011544134.1:n.216+1590C>G
XM_011545833.1:c.216+1590C>G	XP_011544135.1:n.216+1590C>G
XM_011545834.1:c.90+1590C>G	XP_011544136.1:n.90+1590C>G
XM_011545826.2:c.505C>G	XP_011544128.1:p.Pro169Ala
XM_011545827.2:c.505C>G	XP_011544129.1:p.Pro169Ala
XM_011545828.2:c.238C>G	XP_011544130.1:p.Pro80Ala
XM_011545830.2:c.216+1590C>G	XP_011544132.1:n.216+1590C>G
XM_011545833.2:c.216+1590C>G	XP_011544135.1:n.216+1590C>G
XM_011545834.2:c.90+1590C>G	XP_011544136.1:n.90+1590C>G
XM_017023211.1:c.505C>G	XP_016878700.1:p.Pro169Ala
NM_000418.4:c.505C>G MANE Select	NP_000409.1:p.Pro169Ala
NM_001257406.2:c.505C>G	NP_001244335.1:p.Pro169Ala
NM_001257407.2:c.460C>G	NP_001244336.1:p.Pro154Ala
NM_001257997.2:c.30C>G	NP_001244926.1:p.Thr10=