Canonical Allele Identifier: CA360944495

Gene: IL13

Linked Data

• MyVariant Identifiers: chr5:g.131995975A>C (hg19) ; chr5:g.132660283A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132660283A>C , CM000667.2:g.132660283A>C	GRCh38
NC_000005.9:g.131995975A>C , CM000667.1:g.131995975A>C	GRCh37
NC_000005.8:g.132023874A>C	NCBI36
NG_012090.1:g.7111A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304506.7:c.*1A>C MANE Select	ENSP00000304915.3:n.*1A>C
ENST00000459878.5:n.446A>C
ENST00000462480.1:n.1513A>C
ENST00000468334.5:n.815A>C
ENST00000487267.5:n.613A>C
ENST00000617259.2:c.397A>C	ENSP00000479835.1:p.Asn133His
NM_002188.2:c.*1A>C	NP_002179.2:n.*1A>C
NM_001354991.1:c.*1A>C	NP_001341920.1:n.*1A>C
NM_001354992.1:c.*1A>C	NP_001341921.1:n.*1A>C
NM_001354993.1:c.*1A>C	NP_001341922.1:n.*1A>C
NM_002188.3:c.*1A>C MANE Select	NP_002179.2:n.*1A>C
NM_001354991.2:c.*1A>C	NP_001341920.1:n.*1A>C
NM_001354992.2:c.*1A>C	NP_001341921.1:n.*1A>C
NM_001354993.2:c.*1A>C	NP_001341922.1:n.*1A>C