Canonical Allele Identifier: CA360944448

Gene: IL13

Linked Data

• MyVariant Identifiers: chr5:g.131995970A>T (hg19) ; chr5:g.132660278A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132660278A>T , CM000667.2:g.132660278A>T	GRCh38
NC_000005.9:g.131995970A>T , CM000667.1:g.131995970A>T	GRCh37
NC_000005.8:g.132023869A>T	NCBI36
NG_012090.1:g.7106A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304506.7:c.437A>T MANE Select	ENSP00000304915.3:p.Asn146Ile
ENST00000459878.5:n.441A>T
ENST00000462480.1:n.1508A>T
ENST00000468334.5:n.810A>T
ENST00000487267.5:n.608A>T
ENST00000617259.2:c.395A>T	ENSP00000479835.1:p.Asn132Ile
NM_002188.2:c.437A>T	NP_002179.2:p.Asn146Ile
NM_001354991.1:c.242A>T	NP_001341920.1:p.Asn81Ile
NM_001354992.1:c.242A>T	NP_001341921.1:p.Asn81Ile
NM_001354993.1:c.242A>T	NP_001341922.1:p.Asn81Ile
NM_002188.3:c.437A>T MANE Select	NP_002179.2:p.Asn146Ile
NM_001354991.2:c.242A>T	NP_001341920.1:p.Asn81Ile
NM_001354992.2:c.242A>T	NP_001341921.1:p.Asn81Ile
NM_001354993.2:c.242A>T	NP_001341922.1:p.Asn81Ile