Canonical Allele Identifier: CA360944412

Gene: IL13

Linked Data

• MyVariant Identifiers: chr5:g.131995968C>A (hg19) ; chr5:g.132660276C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132660276C>A , CM000667.2:g.132660276C>A	GRCh38
NC_000005.9:g.131995968C>A , CM000667.1:g.131995968C>A	GRCh37
NC_000005.8:g.132023867C>A	NCBI36
NG_012090.1:g.7104C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304506.7:c.435C>A MANE Select	ENSP00000304915.3:p.Phe145Leu
ENST00000459878.5:n.439C>A
ENST00000462480.1:n.1506C>A
ENST00000468334.5:n.808C>A
ENST00000487267.5:n.606C>A
ENST00000617259.2:c.393C>A	ENSP00000479835.1:p.Phe131Leu
NM_002188.2:c.435C>A	NP_002179.2:p.Phe145Leu
NM_001354991.1:c.240C>A	NP_001341920.1:p.Phe80Leu
NM_001354992.1:c.240C>A	NP_001341921.1:p.Phe80Leu
NM_001354993.1:c.240C>A	NP_001341922.1:p.Phe80Leu
NM_002188.3:c.435C>A MANE Select	NP_002179.2:p.Phe145Leu
NM_001354991.2:c.240C>A	NP_001341920.1:p.Phe80Leu
NM_001354992.2:c.240C>A	NP_001341921.1:p.Phe80Leu
NM_001354993.2:c.240C>A	NP_001341922.1:p.Phe80Leu