Canonical Allele Identifier: CA804011370

Gene: IL13

Linked Data

• dbSNP Id: rs1160914308
• MyVariant Identifiers: chr5:g.131993387_131993390del (hg19) ; chr5:g.132657695_132657698del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132657698_132657701del , CM000667.2:g.132657698_132657701del	GRCh38
NC_000005.9:g.131993390_131993393del , CM000667.1:g.131993390_131993393del	GRCh37
NC_000005.8:g.132021289_132021292del	NCBI36
NG_012090.1:g.4526_4529del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000459878.5:n.108-592_108-589del
ENST00000468334.5:n.547+454_547+457del
ENST00000487267.5:n.274+454_274+457del
NM_001354991.1:c.-92-592_-92-589del	NP_001341920.1:n.-92-592_-92-589del
NM_001354992.1:c.-93+454_-93+457del	NP_001341921.1:n.-93+454_-93+457del
NM_001354993.1:c.-22+454_-22+457del	NP_001341922.1:n.-22+454_-22+457del
NM_001354991.2:c.-92-592_-92-589del	NP_001341920.1:n.-92-592_-92-589del
NM_001354992.2:c.-93+454_-93+457del	NP_001341921.1:n.-93+454_-93+457del
NM_001354993.2:c.-22+454_-22+457del	NP_001341922.1:n.-22+454_-22+457del