Canonical Allele Identifier: CA2149671023
Gene: DIO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.80203252C= , CM000676.2:g.80203252C= GRCh38
NC_000014.8:g.80669595C= , CM000676.1:g.80669595C= GRCh37
NC_000014.7:g.79739348C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000438257.9:c.259G= MANE Select ENSP00000405854.5:p.Val87=
ENST00000555750.2:c.*97G= ENSP00000450980.2:n.*97G=
ENST00000422005.7:c.*60G= ENSP00000411438.4:n.*60G=
ENST00000438257.8:c.259G= ENSP00000405854.4:p.Val87=
ENST00000555750.1:c.367G= ENSP00000450980.1:p.Val123=
ENST00000555844.1:c.343G=
ENST00000556811.5:c.235G=
ENST00000557010.5:c.259G= ENSP00000451419.1:p.Val87=
ENST00000557125.1:c.49-166G= ENSP00000450547.1:n.49-166G=
NM_000793.5:c.259G= NP_000784.2:p.Val87=
NM_001007023.3:c.367G= NP_001007024.1:p.Val123=
NM_001242502.1:c.*60G= NP_001229431.1:n.*60G=
NM_001242503.1:c.*60G= NP_001229432.1:n.*60G=
NM_013989.4:c.259G= NP_054644.1:p.Val87=
NM_000793.6:c.259G= NP_000784.3:p.Val87=
NM_001324462.2:c.259G= NP_001311391.2:p.Val87=
NM_001366496.1:c.259G= NP_001353425.1:p.Val87=
NM_013989.5:c.259G= MANE Select NP_054644.1:p.Val87=
NR_158990.1:n.399G=
NR_158991.1:n.533G=