Canonical Allele Identifier: CA390765392

Gene: DIO2

Linked Data

• MyVariant Identifiers: chr14:g.80669567T>A (hg19) ; chr14:g.80203224T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.80203224T>A , CM000676.2:g.80203224T>A	GRCh38
NC_000014.8:g.80669567T>A , CM000676.1:g.80669567T>A	GRCh37
NC_000014.7:g.79739320T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438257.9:c.287A>T MANE Select	ENSP00000405854.5:p.Asp96Val
ENST00000555750.2:c.*125A>T	ENSP00000450980.2:n.*125A>T
ENST00000422005.7:c.*88A>T	ENSP00000411438.4:n.*88A>T
ENST00000438257.8:c.287A>T	ENSP00000405854.4:p.Asp96Val
ENST00000555750.1:c.395A>T	ENSP00000450980.1:p.Asp132Val
ENST00000555844.1:c.371A>T
ENST00000556811.5:c.263A>T
ENST00000557010.5:c.287A>T	ENSP00000451419.1:p.Asp96Val
ENST00000557125.1:c.49-138A>T	ENSP00000450547.1:n.49-138A>T
NM_000793.5:c.287A>T	NP_000784.2:p.Asp96Val
NM_001007023.3:c.395A>T	NP_001007024.1:p.Asp132Val
NM_001242502.1:c.*88A>T	NP_001229431.1:n.*88A>T
NM_001242503.1:c.*88A>T	NP_001229432.1:n.*88A>T
NM_013989.4:c.287A>T	NP_054644.1:p.Asp96Val
NM_000793.6:c.287A>T	NP_000784.3:p.Asp96Val
NM_001324462.2:c.287A>T	NP_001311391.2:p.Asp96Val
NM_001366496.1:c.287A>T	NP_001353425.1:p.Asp96Val
NM_013989.5:c.287A>T MANE Select	NP_054644.1:p.Asp96Val
NR_158990.1:n.427A>T
NR_158991.1:n.561A>T