Canonical Allele Identifier: CA360944479

Gene: IL13

Linked Data

• MyVariant Identifiers: chr5:g.131995973G>A (hg19) ; chr5:g.132660281G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132660281G>A , CM000667.2:g.132660281G>A	GRCh38
NC_000005.9:g.131995973G>A , CM000667.1:g.131995973G>A	GRCh37
NC_000005.8:g.132023872G>A	NCBI36
NG_012090.1:g.7109G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304506.7:c.440G>A MANE Select	ENSP00000304915.3:p.Ter147=
ENST00000459878.5:n.444G>A
ENST00000462480.1:n.1511G>A
ENST00000468334.5:n.813G>A
ENST00000487267.5:n.611G>A
ENST00000617259.2:c.397-2G>A	ENSP00000479835.1:n.397-2G>A
NM_002188.2:c.440G>A	NP_002179.2:p.Ter147=
NM_001354991.1:c.245G>A	NP_001341920.1:p.Ter82=
NM_001354992.1:c.245G>A	NP_001341921.1:p.Ter82=
NM_001354993.1:c.245G>A	NP_001341922.1:p.Ter82=
NM_002188.3:c.440G>A MANE Select	NP_002179.2:p.Ter147=
NM_001354991.2:c.245G>A	NP_001341920.1:p.Ter82=
NM_001354992.2:c.245G>A	NP_001341921.1:p.Ter82=
NM_001354993.2:c.245G>A	NP_001341922.1:p.Ter82=