Canonical Allele Identifier: CA487516768
Gene: DIO2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.80669602G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.80203259G>A , CM000676.2:g.80203259G>A GRCh38
NC_000014.8:g.80669602G>A , CM000676.1:g.80669602G>A GRCh37
NC_000014.7:g.79739355G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000438257.9:c.252C>T MANE Select ENSP00000405854.5:p.Ser84=
ENST00000555750.2:c.*90C>T ENSP00000450980.2:n.*90C>T
ENST00000422005.7:c.*53C>T ENSP00000411438.4:n.*53C>T
ENST00000438257.8:c.252C>T ENSP00000405854.4:p.Ser84=
ENST00000555750.1:c.360C>T ENSP00000450980.1:p.Ser120=
ENST00000555844.1:c.336C>T
ENST00000556811.5:c.228C>T
ENST00000557010.5:c.252C>T ENSP00000451419.1:p.Ser84=
ENST00000557125.1:c.49-173C>T ENSP00000450547.1:n.49-173C>T
NM_000793.5:c.252C>T NP_000784.2:p.Ser84=
NM_001007023.3:c.360C>T NP_001007024.1:p.Ser120=
NM_001242502.1:c.*53C>T NP_001229431.1:n.*53C>T
NM_001242503.1:c.*53C>T NP_001229432.1:n.*53C>T
NM_013989.4:c.252C>T NP_054644.1:p.Ser84=
NM_000793.6:c.252C>T NP_000784.3:p.Ser84=
NM_001324462.2:c.252C>T NP_001311391.2:p.Ser84=
NM_001366496.1:c.252C>T NP_001353425.1:p.Ser84=
NM_013989.5:c.252C>T MANE Select NP_054644.1:p.Ser84=
NR_158990.1:n.392C>T
NR_158991.1:n.526C>T