Canonical Allele Identifier: CA2123434607
Gene: IL25 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375604_23375607delinsTGAC , CM000676.2:g.23375604_23375607delinsTGAC GRCh38
NC_000014.8:g.23844813_23844816delinsTGAC , CM000676.1:g.23844813_23844816delinsTGAC GRCh37
NC_000014.7:g.22914653_22914656delinsTGAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.231-21_231-18delinsTGAC MANE Select ENSP00000380417.2:n.231-21_231-18delinsTGAC
ENST00000329715.2:c.279-21_279-18delinsTGAC ENSP00000328111.2:n.279-21_279-18delinsTGAC
ENST00000397242.2:c.231-21_231-18delinsTGAC ENSP00000380417.2:n.231-21_231-18delinsTGAC
NM_022789.3:c.279-21_279-18delinsTGAC NP_073626.1:n.279-21_279-18delinsTGAC
NM_172314.1:c.231-21_231-18delinsTGAC NP_758525.1:n.231-21_231-18delinsTGAC