Canonical Allele Identifier: CA1583263229

Gene: IL13

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132660275T= , CM000667.2:g.132660275T=	GRCh38
NC_000005.9:g.131995967T= , CM000667.1:g.131995967T=	GRCh37
NC_000005.8:g.132023866T=	NCBI36
NG_012090.1:g.7103T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304506.7:c.434T= MANE Select	ENSP00000304915.3:p.Phe145=
ENST00000459878.5:n.438T=
ENST00000462480.1:n.1505T=
ENST00000468334.5:n.807T=
ENST00000487267.5:n.605T=
ENST00000617259.2:c.392T=	ENSP00000479835.1:p.Phe131=
NM_002188.2:c.434T=	NP_002179.2:p.Phe145=
NM_001354991.1:c.239T=	NP_001341920.1:p.Phe80=
NM_001354992.1:c.239T=	NP_001341921.1:p.Phe80=
NM_001354993.1:c.239T=	NP_001341922.1:p.Phe80=
NM_002188.3:c.434T= MANE Select	NP_002179.2:p.Phe145=
NM_001354991.2:c.239T=	NP_001341920.1:p.Phe80=
NM_001354992.2:c.239T=	NP_001341921.1:p.Phe80=
NM_001354993.2:c.239T=	NP_001341922.1:p.Phe80=