Canonical Allele Identifier: CA360944463

Gene: IL13

Linked Data

• MyVariant Identifiers: chr5:g.131995971C>G (hg19) ; chr5:g.132660279C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132660279C>G , CM000667.2:g.132660279C>G	GRCh38
NC_000005.9:g.131995971C>G , CM000667.1:g.131995971C>G	GRCh37
NC_000005.8:g.132023870C>G	NCBI36
NG_012090.1:g.7107C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000304506.7:c.438C>G MANE Select	ENSP00000304915.3:p.Asn146Lys
ENST00000459878.5:n.442C>G
ENST00000462480.1:n.1509C>G
ENST00000468334.5:n.811C>G
ENST00000487267.5:n.609C>G
ENST00000617259.2:c.396C>G	ENSP00000479835.1:p.Asn132Lys
NM_002188.2:c.438C>G	NP_002179.2:p.Asn146Lys
NM_001354991.1:c.243C>G	NP_001341920.1:p.Asn81Lys
NM_001354992.1:c.243C>G	NP_001341921.1:p.Asn81Lys
NM_001354993.1:c.243C>G	NP_001341922.1:p.Asn81Lys
NM_002188.3:c.438C>G MANE Select	NP_002179.2:p.Asn146Lys
NM_001354991.2:c.243C>G	NP_001341920.1:p.Asn81Lys
NM_001354992.2:c.243C>G	NP_001341921.1:p.Asn81Lys
NM_001354993.2:c.243C>G	NP_001341922.1:p.Asn81Lys