Canonical Allele Identifier: CA390765143

Gene: DIO2

Linked Data

• MyVariant Identifiers: chr14:g.80669451G>T (hg19) ; chr14:g.80203108G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.80203108G>T , CM000676.2:g.80203108G>T	GRCh38
NC_000014.8:g.80669451G>T , CM000676.1:g.80669451G>T	GRCh37
NC_000014.7:g.79739204G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438257.9:c.403C>A MANE Select	ENSP00000405854.5:p.Pro135Thr
ENST00000555750.2:c.*241C>A	ENSP00000450980.2:n.*241C>A
ENST00000422005.7:c.*204C>A	ENSP00000411438.4:n.*204C>A
ENST00000438257.8:c.403C>A	ENSP00000405854.4:p.Pro135Thr
ENST00000555750.1:c.511C>A	ENSP00000450980.1:p.Pro171Thr
ENST00000555844.1:c.487C>A
ENST00000556811.5:c.379C>A
ENST00000557010.5:c.403C>A	ENSP00000451419.1:p.Pro135Thr
ENST00000557125.1:c.49-22C>A	ENSP00000450547.1:n.49-22C>A
NM_000793.5:c.403C>A	NP_000784.2:p.Pro135Thr
NM_001007023.3:c.511C>A	NP_001007024.1:p.Pro171Thr
NM_001242502.1:c.*204C>A	NP_001229431.1:n.*204C>A
NM_001242503.1:c.*204C>A	NP_001229432.1:n.*204C>A
NM_013989.4:c.403C>A	NP_054644.1:p.Pro135Thr
NM_000793.6:c.403C>A	NP_000784.3:p.Pro135Thr
NM_001324462.2:c.403C>A	NP_001311391.2:p.Pro135Thr
NM_001366496.1:c.403C>A	NP_001353425.1:p.Pro135Thr
NM_013989.5:c.403C>A MANE Select	NP_054644.1:p.Pro135Thr
NR_158990.1:n.543C>A
NR_158991.1:n.677C>A