Canonical Allele Identifier: CA1583262042
Gene: IL13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132657590_132657591delinsCT , CM000667.2:g.132657590_132657591delinsCT GRCh38
NC_000005.9:g.131993282_131993283delinsCT , CM000667.1:g.131993282_131993283delinsCT GRCh37
NC_000005.8:g.132021181_132021182delinsCT NCBI36
NG_012090.1:g.4418_4419delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000459878.5:n.108-700_108-699delinsCT
ENST00000468334.5:n.547+346_547+347delinsCT
ENST00000487267.5:n.274+346_274+347delinsCT
NM_001354991.1:c.-92-700_-92-699delinsCT NP_001341920.1:n.-92-700_-92-699delinsCT
NM_001354992.1:c.-93+346_-93+347delinsCT NP_001341921.1:n.-93+346_-93+347delinsCT
NM_001354993.1:c.-22+346_-22+347delinsCT NP_001341922.1:n.-22+346_-22+347delinsCT
NM_001354991.2:c.-92-700_-92-699delinsCT NP_001341920.1:n.-92-700_-92-699delinsCT
NM_001354992.2:c.-93+346_-93+347delinsCT NP_001341921.1:n.-93+346_-93+347delinsCT
NM_001354993.2:c.-22+346_-22+347delinsCT NP_001341922.1:n.-22+346_-22+347delinsCT