Canonical Allele Identifier: CA360944488

Gene: IL13

Linked Data

• MyVariant Identifiers: chr5:g.131995974A>C (hg19) ; chr5:g.132660282A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132660282A>C , CM000667.2:g.132660282A>C	GRCh38
NC_000005.9:g.131995974A>C , CM000667.1:g.131995974A>C	GRCh37
NC_000005.8:g.132023873A>C	NCBI36
NG_012090.1:g.7110A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000304506.7:c.441A>C MANE Select	ENSP00000304915.3:p.Ter147Cys
ENST00000459878.5:n.445A>C
ENST00000462480.1:n.1512A>C
ENST00000468334.5:n.814A>C
ENST00000487267.5:n.612A>C
ENST00000617259.2:c.397-1A>C	ENSP00000479835.1:n.397-1A>C
NM_002188.2:c.441A>C	NP_002179.2:p.Ter147Cys
NM_001354991.1:c.246A>C	NP_001341920.1:p.Ter82Cys
NM_001354992.1:c.246A>C	NP_001341921.1:p.Ter82Cys
NM_001354993.1:c.246A>C	NP_001341922.1:p.Ter82Cys
NM_002188.3:c.441A>C MANE Select	NP_002179.2:p.Ter147Cys
NM_001354991.2:c.246A>C	NP_001341920.1:p.Ter82Cys
NM_001354992.2:c.246A>C	NP_001341921.1:p.Ter82Cys
NM_001354993.2:c.246A>C	NP_001341922.1:p.Ter82Cys