Canonical Allele Identifier: CA360944508

Gene: IL13

Linked Data

• MyVariant Identifiers: chr5:g.131995977C>G (hg19) ; chr5:g.132660285C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132660285C>G , CM000667.2:g.132660285C>G	GRCh38
NC_000005.9:g.131995977C>G , CM000667.1:g.131995977C>G	GRCh37
NC_000005.8:g.132023876C>G	NCBI36
NG_012090.1:g.7113C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304506.7:c.*3C>G MANE Select	ENSP00000304915.3:n.*3C>G
ENST00000459878.5:n.448C>G
ENST00000462480.1:n.1515C>G
ENST00000468334.5:n.817C>G
ENST00000487267.5:n.615C>G
ENST00000617259.2:c.399C>G	ENSP00000479835.1:p.Asn133Lys
NM_002188.2:c.*3C>G	NP_002179.2:n.*3C>G
NM_001354991.1:c.*3C>G	NP_001341920.1:n.*3C>G
NM_001354992.1:c.*3C>G	NP_001341921.1:n.*3C>G
NM_001354993.1:c.*3C>G	NP_001341922.1:n.*3C>G
NM_002188.3:c.*3C>G MANE Select	NP_002179.2:n.*3C>G
NM_001354991.2:c.*3C>G	NP_001341920.1:n.*3C>G
NM_001354992.2:c.*3C>G	NP_001341921.1:n.*3C>G
NM_001354993.2:c.*3C>G	NP_001341922.1:n.*3C>G