Canonical Allele Identifier: CA1583263232

Gene: IL13

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132660283A= , CM000667.2:g.132660283A=	GRCh38
NC_000005.9:g.131995975A= , CM000667.1:g.131995975A=	GRCh37
NC_000005.8:g.132023874A=	NCBI36
NG_012090.1:g.7111A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000304506.7:c.*1A= MANE Select	ENSP00000304915.3:n.*1A=
ENST00000459878.5:n.446A=
ENST00000462480.1:n.1513A=
ENST00000468334.5:n.815A=
ENST00000487267.5:n.613A=
ENST00000617259.2:c.397A=	ENSP00000479835.1:p.Asn133=
NM_002188.2:c.*1A=	NP_002179.2:n.*1A=
NM_001354991.1:c.*1A=	NP_001341920.1:n.*1A=
NM_001354992.1:c.*1A=	NP_001341921.1:n.*1A=
NM_001354993.1:c.*1A=	NP_001341922.1:n.*1A=
NM_002188.3:c.*1A= MANE Select	NP_002179.2:n.*1A=
NM_001354991.2:c.*1A=	NP_001341920.1:n.*1A=
NM_001354992.2:c.*1A=	NP_001341921.1:n.*1A=
NM_001354993.2:c.*1A=	NP_001341922.1:n.*1A=