Canonical Allele Identifier: CA360944381

Gene: IL13

Linked Data

• MyVariant Identifiers: chr5:g.131995966T>A (hg19) ; chr5:g.132660274T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132660274T>A , CM000667.2:g.132660274T>A	GRCh38
NC_000005.9:g.131995966T>A , CM000667.1:g.131995966T>A	GRCh37
NC_000005.8:g.132023865T>A	NCBI36
NG_012090.1:g.7102T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304506.7:c.433T>A MANE Select	ENSP00000304915.3:p.Phe145Ile
ENST00000459878.5:n.437T>A
ENST00000462480.1:n.1504T>A
ENST00000468334.5:n.806T>A
ENST00000487267.5:n.604T>A
ENST00000617259.2:c.391T>A	ENSP00000479835.1:p.Phe131Ile
NM_002188.2:c.433T>A	NP_002179.2:p.Phe145Ile
NM_001354991.1:c.238T>A	NP_001341920.1:p.Phe80Ile
NM_001354992.1:c.238T>A	NP_001341921.1:p.Phe80Ile
NM_001354993.1:c.238T>A	NP_001341922.1:p.Phe80Ile
NM_002188.3:c.433T>A MANE Select	NP_002179.2:p.Phe145Ile
NM_001354991.2:c.238T>A	NP_001341920.1:p.Phe80Ile
NM_001354992.2:c.238T>A	NP_001341921.1:p.Phe80Ile
NM_001354993.2:c.238T>A	NP_001341922.1:p.Phe80Ile