Canonical Allele Identifier: CA2149670748
Gene: DIO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.80203061G= , CM000676.2:g.80203061G= GRCh38
NC_000014.8:g.80669404G= , CM000676.1:g.80669404G= GRCh37
NC_000014.7:g.79739157G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000438257.9:c.450C= MANE Select ENSP00000405854.5:p.Phe150=
ENST00000555750.2:c.*288C= ENSP00000450980.2:n.*288C=
ENST00000422005.7:c.*251C= ENSP00000411438.4:n.*251C=
ENST00000438257.8:c.450C= ENSP00000405854.4:p.Phe150=
ENST00000555750.1:c.558C= ENSP00000450980.1:p.Phe186=
ENST00000555844.1:c.534C=
ENST00000556811.5:c.426C=
ENST00000557010.5:c.450C= ENSP00000451419.1:p.Phe150=
ENST00000557125.1:c.74C= ENSP00000450547.1:p.Ser25=
NM_000793.5:c.450C= NP_000784.2:p.Phe150=
NM_001007023.3:c.558C= NP_001007024.1:p.Phe186=
NM_001242502.1:c.*251C= NP_001229431.1:n.*251C=
NM_001242503.1:c.*251C= NP_001229432.1:n.*251C=
NM_013989.4:c.450C= NP_054644.1:p.Phe150=
NM_000793.6:c.450C= NP_000784.3:p.Phe150=
NM_001324462.2:c.450C= NP_001311391.2:p.Phe150=
NM_001366496.1:c.450C= NP_001353425.1:p.Phe150=
NM_013989.5:c.450C= MANE Select NP_054644.1:p.Phe150=
NR_158990.1:n.590C=
NR_158991.1:n.724C=