Canonical Allele Identifier: CA360944438

Gene: IL13

Linked Data

• gnomAD v4: 5-132660277-A-T
• MyVariant Identifiers: chr5:g.131995969A>T (hg19) ; chr5:g.132660277A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132660277A>T , CM000667.2:g.132660277A>T	GRCh38
NC_000005.9:g.131995969A>T , CM000667.1:g.131995969A>T	GRCh37
NC_000005.8:g.132023868A>T	NCBI36
NG_012090.1:g.7105A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304506.7:c.436A>T MANE Select	ENSP00000304915.3:p.Asn146Tyr
ENST00000459878.5:n.440A>T
ENST00000462480.1:n.1507A>T
ENST00000468334.5:n.809A>T
ENST00000487267.5:n.607A>T
ENST00000617259.2:c.394A>T	ENSP00000479835.1:p.Asn132Tyr
NM_002188.2:c.436A>T	NP_002179.2:p.Asn146Tyr
NM_001354991.1:c.241A>T	NP_001341920.1:p.Asn81Tyr
NM_001354992.1:c.241A>T	NP_001341921.1:p.Asn81Tyr
NM_001354993.1:c.241A>T	NP_001341922.1:p.Asn81Tyr
NM_002188.3:c.436A>T MANE Select	NP_002179.2:p.Asn146Tyr
NM_001354991.2:c.241A>T	NP_001341920.1:p.Asn81Tyr
NM_001354992.2:c.241A>T	NP_001341921.1:p.Asn81Tyr
NM_001354993.2:c.241A>T	NP_001341922.1:p.Asn81Tyr