Canonical Allele Identifier: CA1081656096

Gene: IL13

Linked Data

• gnomAD v3: 5-132660272-A-ATTTTTTTTTTT
• gnomAD v4: 5-132660272-A-ATTTTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132660272_132660273insTTTTTTTTTTT , CM000667.2:g.132660272_132660273insTTTTTTTTTTT	GRCh38
NC_000005.9:g.131995964_131995965insTTTTTTTTTTT , CM000667.1:g.131995964_131995965insTTTTTTTTTTT	GRCh37
NC_000005.8:g.132023863_132023864insTTTTTTTTTTT	NCBI36
NG_012090.1:g.7100_7101insTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304506.7:c.431_432insTTTTTTTTTTT MANE Select	ENSP00000304915.3:p.Gln144HisfsTer23
ENST00000459878.5:n.435_436insTTTTTTTTTTT
ENST00000462480.1:n.1502_1503insTTTTTTTTTTT
ENST00000468334.5:n.804_805insTTTTTTTTTTT
ENST00000487267.5:n.602_603insTTTTTTTTTTT
ENST00000617259.2:c.389_390insTTTTTTTTTTT	ENSP00000479835.1:p.Gln130HisfsTer22
NM_002188.2:c.431_432insTTTTTTTTTTT	NP_002179.2:p.Gln144HisfsTer23
NM_001354991.1:c.236_237insTTTTTTTTTTT	NP_001341920.1:p.Gln79HisfsTer23
NM_001354992.1:c.236_237insTTTTTTTTTTT	NP_001341921.1:p.Gln79HisfsTer23
NM_001354993.1:c.236_237insTTTTTTTTTTT	NP_001341922.1:p.Gln79HisfsTer23
NM_002188.3:c.431_432insTTTTTTTTTTT MANE Select	NP_002179.2:p.Gln144HisfsTer23
NM_001354991.2:c.236_237insTTTTTTTTTTT	NP_001341920.1:p.Gln79HisfsTer23
NM_001354992.2:c.236_237insTTTTTTTTTTT	NP_001341921.1:p.Gln79HisfsTer23
NM_001354993.2:c.236_237insTTTTTTTTTTT	NP_001341922.1:p.Gln79HisfsTer23