Canonical Allele Identifier: CA390765400

Gene: DIO2

Linked Data

• gnomAD v4: 14-80203227-C-A
• MyVariant Identifiers: chr14:g.80669570C>A (hg19) ; chr14:g.80203227C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.80203227C>A , CM000676.2:g.80203227C>A	GRCh38
NC_000014.8:g.80669570C>A , CM000676.1:g.80669570C>A	GRCh37
NC_000014.7:g.79739323C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438257.9:c.284G>T MANE Select	ENSP00000405854.5:p.Gly95Val
ENST00000555750.2:c.*122G>T	ENSP00000450980.2:n.*122G>T
ENST00000422005.7:c.*85G>T	ENSP00000411438.4:n.*85G>T
ENST00000438257.8:c.284G>T	ENSP00000405854.4:p.Gly95Val
ENST00000555750.1:c.392G>T	ENSP00000450980.1:p.Gly131Val
ENST00000555844.1:c.368G>T
ENST00000556811.5:c.260G>T
ENST00000557010.5:c.284G>T	ENSP00000451419.1:p.Gly95Val
ENST00000557125.1:c.49-141G>T	ENSP00000450547.1:n.49-141G>T
NM_000793.5:c.284G>T	NP_000784.2:p.Gly95Val
NM_001007023.3:c.392G>T	NP_001007024.1:p.Gly131Val
NM_001242502.1:c.*85G>T	NP_001229431.1:n.*85G>T
NM_001242503.1:c.*85G>T	NP_001229432.1:n.*85G>T
NM_013989.4:c.284G>T	NP_054644.1:p.Gly95Val
NM_000793.6:c.284G>T	NP_000784.3:p.Gly95Val
NM_001324462.2:c.284G>T	NP_001311391.2:p.Gly95Val
NM_001366496.1:c.284G>T	NP_001353425.1:p.Gly95Val
NM_013989.5:c.284G>T MANE Select	NP_054644.1:p.Gly95Val
NR_158990.1:n.424G>T
NR_158991.1:n.558G>T