Canonical Allele Identifier: CA1583263234

Gene: IL13

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132660285C= , CM000667.2:g.132660285C=	GRCh38
NC_000005.9:g.131995977C= , CM000667.1:g.131995977C=	GRCh37
NC_000005.8:g.132023876C=	NCBI36
NG_012090.1:g.7113C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000304506.7:c.*3C= MANE Select	ENSP00000304915.3:n.*3C=
ENST00000459878.5:n.448C=
ENST00000462480.1:n.1515C=
ENST00000468334.5:n.817C=
ENST00000487267.5:n.615C=
ENST00000617259.2:c.399C=	ENSP00000479835.1:p.Asn133=
NM_002188.2:c.*3C=	NP_002179.2:n.*3C=
NM_001354991.1:c.*3C=	NP_001341920.1:n.*3C=
NM_001354992.1:c.*3C=	NP_001341921.1:n.*3C=
NM_001354993.1:c.*3C=	NP_001341922.1:n.*3C=
NM_002188.3:c.*3C= MANE Select	NP_002179.2:n.*3C=
NM_001354991.2:c.*3C=	NP_001341920.1:n.*3C=
NM_001354992.2:c.*3C=	NP_001341921.1:n.*3C=
NM_001354993.2:c.*3C=	NP_001341922.1:n.*3C=