Canonical Allele Identifier: CA390765458

Gene: DIO2

Linked Data

• gnomAD v4: 14-80203255-C-T
• MyVariant Identifiers: chr14:g.80669598C>T (hg19) ; chr14:g.80203255C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.80203255C>T , CM000676.2:g.80203255C>T	GRCh38
NC_000014.8:g.80669598C>T , CM000676.1:g.80669598C>T	GRCh37
NC_000014.7:g.79739351C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000438257.9:c.256G>A MANE Select	ENSP00000405854.5:p.Val86Met
ENST00000555750.2:c.*94G>A	ENSP00000450980.2:n.*94G>A
ENST00000422005.7:c.*57G>A	ENSP00000411438.4:n.*57G>A
ENST00000438257.8:c.256G>A	ENSP00000405854.4:p.Val86Met
ENST00000555750.1:c.364G>A	ENSP00000450980.1:p.Val122Met
ENST00000555844.1:c.340G>A
ENST00000556811.5:c.232G>A
ENST00000557010.5:c.256G>A	ENSP00000451419.1:p.Val86Met
ENST00000557125.1:c.49-169G>A	ENSP00000450547.1:n.49-169G>A
NM_000793.5:c.256G>A	NP_000784.2:p.Val86Met
NM_001007023.3:c.364G>A	NP_001007024.1:p.Val122Met
NM_001242502.1:c.*57G>A	NP_001229431.1:n.*57G>A
NM_001242503.1:c.*57G>A	NP_001229432.1:n.*57G>A
NM_013989.4:c.256G>A	NP_054644.1:p.Val86Met
NM_000793.6:c.256G>A	NP_000784.3:p.Val86Met
NM_001324462.2:c.256G>A	NP_001311391.2:p.Val86Met
NM_001366496.1:c.256G>A	NP_001353425.1:p.Val86Met
NM_013989.5:c.256G>A MANE Select	NP_054644.1:p.Val86Met
NR_158990.1:n.396G>A
NR_158991.1:n.530G>A