Canonical Allele Identifier: CA2123434635
Gene: IL25 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375631_23375633delinsCAG , CM000676.2:g.23375631_23375633delinsCAG GRCh38
NC_000014.8:g.23844840_23844842delinsCAG , CM000676.1:g.23844840_23844842delinsCAG GRCh37
NC_000014.7:g.22914680_22914682delinsCAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.237_239delinsCAG MANE Select ENSP00000380417.2:p.Asp79=
ENST00000329715.2:c.285_287delinsCAG ENSP00000328111.2:p.Asp95=
ENST00000397242.2:c.237_239delinsCAG ENSP00000380417.2:p.Asp79=
NM_022789.3:c.285_287delinsCAG NP_073626.1:p.Asp95=
NM_172314.1:c.237_239delinsCAG NP_758525.1:p.Asp79=
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