Canonical Allele Identifier: CA1583262038
Gene: IL13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132657584_132657589delinsTCTGAA , CM000667.2:g.132657584_132657589delinsTCTGAA GRCh38
NC_000005.9:g.131993276_131993281delinsTCTGAA , CM000667.1:g.131993276_131993281delinsTCTGAA GRCh37
NC_000005.8:g.132021175_132021180delinsTCTGAA NCBI36
NG_012090.1:g.4412_4417delinsTCTGAA

Transcript Alleles

HGVS Amino-acid change
ENST00000459878.5:n.108-706_108-701delinsTCTGAA
ENST00000468334.5:n.547+340_547+345delinsTCTGAA
ENST00000487267.5:n.274+340_274+345delinsTCTGAA
NM_001354991.1:c.-92-706_-92-701delinsTCTGAA NP_001341920.1:n.-92-706_-92-701delinsTCTGAA
NM_001354992.1:c.-93+340_-93+345delinsTCTGAA NP_001341921.1:n.-93+340_-93+345delinsTCTGAA
NM_001354993.1:c.-22+340_-22+345delinsTCTGAA NP_001341922.1:n.-22+340_-22+345delinsTCTGAA
NM_001354991.2:c.-92-706_-92-701delinsTCTGAA NP_001341920.1:n.-92-706_-92-701delinsTCTGAA
NM_001354992.2:c.-93+340_-93+345delinsTCTGAA NP_001341921.1:n.-93+340_-93+345delinsTCTGAA
NM_001354993.2:c.-22+340_-22+345delinsTCTGAA NP_001341922.1:n.-22+340_-22+345delinsTCTGAA