Canonical Allele Identifier: CA360944473

Gene: IL13

Linked Data

• MyVariant Identifiers: chr5:g.131995972T>G (hg19) ; chr5:g.132660280T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132660280T>G , CM000667.2:g.132660280T>G	GRCh38
NC_000005.9:g.131995972T>G , CM000667.1:g.131995972T>G	GRCh37
NC_000005.8:g.132023871T>G	NCBI36
NG_012090.1:g.7108T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304506.7:c.439T>G MANE Select	ENSP00000304915.3:p.Ter147Gly
ENST00000459878.5:n.443T>G
ENST00000462480.1:n.1510T>G
ENST00000468334.5:n.812T>G
ENST00000487267.5:n.610T>G
ENST00000617259.2:c.396+1T>G	ENSP00000479835.1:n.396+1T>G
NM_002188.2:c.439T>G	NP_002179.2:p.Ter147Gly
NM_001354991.1:c.244T>G	NP_001341920.1:p.Ter82Gly
NM_001354992.1:c.244T>G	NP_001341921.1:p.Ter82Gly
NM_001354993.1:c.244T>G	NP_001341922.1:p.Ter82Gly
NM_002188.3:c.439T>G MANE Select	NP_002179.2:p.Ter147Gly
NM_001354991.2:c.244T>G	NP_001341920.1:p.Ter82Gly
NM_001354992.2:c.244T>G	NP_001341921.1:p.Ter82Gly
NM_001354993.2:c.244T>G	NP_001341922.1:p.Ter82Gly