Canonical Allele Identifier: CA390765250

Gene: DIO2

Linked Data

• MyVariant Identifiers: chr14:g.80669502C>A (hg19) ; chr14:g.80203159C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.80203159C>A , CM000676.2:g.80203159C>A	GRCh38
NC_000014.8:g.80669502C>A , CM000676.1:g.80669502C>A	GRCh37
NC_000014.7:g.79739255C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438257.9:c.352G>T MANE Select	ENSP00000405854.5:p.Ala118Ser
ENST00000555750.2:c.*190G>T	ENSP00000450980.2:n.*190G>T
ENST00000422005.7:c.*153G>T	ENSP00000411438.4:n.*153G>T
ENST00000438257.8:c.352G>T	ENSP00000405854.4:p.Ala118Ser
ENST00000555750.1:c.460G>T	ENSP00000450980.1:p.Ala154Ser
ENST00000555844.1:c.436G>T
ENST00000556811.5:c.328G>T
ENST00000557010.5:c.352G>T	ENSP00000451419.1:p.Ala118Ser
ENST00000557125.1:c.49-73G>T	ENSP00000450547.1:n.49-73G>T
NM_000793.5:c.352G>T	NP_000784.2:p.Ala118Ser
NM_001007023.3:c.460G>T	NP_001007024.1:p.Ala154Ser
NM_001242502.1:c.*153G>T	NP_001229431.1:n.*153G>T
NM_001242503.1:c.*153G>T	NP_001229432.1:n.*153G>T
NM_013989.4:c.352G>T	NP_054644.1:p.Ala118Ser
NM_000793.6:c.352G>T	NP_000784.3:p.Ala118Ser
NM_001324462.2:c.352G>T	NP_001311391.2:p.Ala118Ser
NM_001366496.1:c.352G>T	NP_001353425.1:p.Ala118Ser
NM_013989.5:c.352G>T MANE Select	NP_054644.1:p.Ala118Ser
NR_158990.1:n.492G>T
NR_158991.1:n.626G>T