Canonical Allele Identifier: CA1583262514

Gene: IL13

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132658743C= , CM000667.2:g.132658743C=	GRCh38
NC_000005.9:g.131994435C= , CM000667.1:g.131994435C=	GRCh37
NC_000005.8:g.132022334C=	NCBI36
NG_012090.1:g.5571C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304506.7:c.174+383C= MANE Select	ENSP00000304915.3:n.174+383C=
ENST00000459878.5:n.178+383C=
ENST00000462480.1:n.571C=
ENST00000468334.5:n.548-675C=
ENST00000487267.5:n.345+383C=
ENST00000617259.2:c.132+383C=	ENSP00000479835.1:n.132+383C=
NM_002188.2:c.174+383C=	NP_002179.2:n.174+383C=
NM_001354991.1:c.-22+383C=	NP_001341920.1:n.-22+383C=
NM_001354992.1:c.-22+383C=	NP_001341921.1:n.-22+383C=
NM_001354993.1:c.-21-675C=	NP_001341922.1:n.-21-675C=
NM_002188.3:c.174+383C= MANE Select	NP_002179.2:n.174+383C=
NM_001354991.2:c.-22+383C=	NP_001341920.1:n.-22+383C=
NM_001354992.2:c.-22+383C=	NP_001341921.1:n.-22+383C=
NM_001354993.2:c.-21-675C=	NP_001341922.1:n.-21-675C=