Canonical Allele Identifier: CA2149673386
Gene: DIO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.80205776C= , CM000676.2:g.80205776C= GRCh38
NC_000014.8:g.80672119C= , CM000676.1:g.80672119C= GRCh37
NC_000014.7:g.79741872C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000438257.9:c.223-2488G= MANE Select ENSP00000405854.5:n.223-2488G=
ENST00000555750.2:c.*60+455G= ENSP00000450980.2:n.*60+455G=
ENST00000422005.7:c.328-41G= ENSP00000411438.4:n.328-41G=
ENST00000438257.8:c.223-2488G= ENSP00000405854.4:n.223-2488G=
ENST00000555750.1:c.330+455G= ENSP00000450980.1:n.330+455G=
ENST00000555844.1:c.173-41G=
ENST00000556811.5:c.65-41G=
ENST00000557010.5:c.223-2488G= ENSP00000451419.1:n.223-2488G=
ENST00000557125.1:c.49-2690G= ENSP00000450547.1:n.49-2690G=
NM_000793.5:c.223-2488G= NP_000784.2:n.223-2488G=
NM_001007023.3:c.330+455G= NP_001007024.1:n.330+455G=
NM_001242502.1:c.331-41G= NP_001229431.1:n.331-41G=
NM_001242503.1:c.223-41G= NP_001229432.1:n.223-41G=
NM_013989.4:c.223-2488G= NP_054644.1:n.223-2488G=
NM_000793.6:c.223-2488G= NP_000784.3:n.223-2488G=
NM_001324462.2:c.223-2488G= NP_001311391.2:n.223-2488G=
NM_001366496.1:c.223-2488G= NP_001353425.1:n.223-2488G=
NM_013989.5:c.223-2488G= MANE Select NP_054644.1:n.223-2488G=
NR_158990.1:n.362+455G=
NR_158991.1:n.363-41G=