Canonical Allele Identifier: CA487516839

Gene: DIO2

Linked Data

• MyVariant Identifiers: chr14:g.80669437C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.80203094C>T , CM000676.2:g.80203094C>T	GRCh38
NC_000014.8:g.80669437C>T , CM000676.1:g.80669437C>T	GRCh37
NC_000014.7:g.79739190C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438257.9:c.417G>A MANE Select	ENSP00000405854.5:p.Gln139=
ENST00000555750.2:c.*255G>A	ENSP00000450980.2:n.*255G>A
ENST00000422005.7:c.*218G>A	ENSP00000411438.4:n.*218G>A
ENST00000438257.8:c.417G>A	ENSP00000405854.4:p.Gln139=
ENST00000555750.1:c.525G>A	ENSP00000450980.1:p.Gln175=
ENST00000555844.1:c.501G>A
ENST00000556811.5:c.393G>A
ENST00000557010.5:c.417G>A	ENSP00000451419.1:p.Gln139=
ENST00000557125.1:c.49-8G>A	ENSP00000450547.1:n.49-8G>A
NM_000793.5:c.417G>A	NP_000784.2:p.Gln139=
NM_001007023.3:c.525G>A	NP_001007024.1:p.Gln175=
NM_001242502.1:c.*218G>A	NP_001229431.1:n.*218G>A
NM_001242503.1:c.*218G>A	NP_001229432.1:n.*218G>A
NM_013989.4:c.417G>A	NP_054644.1:p.Gln139=
NM_000793.6:c.417G>A	NP_000784.3:p.Gln139=
NM_001324462.2:c.417G>A	NP_001311391.2:p.Gln139=
NM_001366496.1:c.417G>A	NP_001353425.1:p.Gln139=
NM_013989.5:c.417G>A MANE Select	NP_054644.1:p.Gln139=
NR_158990.1:n.557G>A
NR_158991.1:n.691G>A