Canonical Allele Identifier: CA487516500

Gene: DIO2

Linked Data

• COSMIC: COSM1135623 ; COSM1135624
• MyVariant Identifiers: chr14:g.80669284A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.80202941A>G , CM000676.2:g.80202941A>G	GRCh38
NC_000014.8:g.80669284A>G , CM000676.1:g.80669284A>G	GRCh37
NC_000014.7:g.79739037A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438257.9:c.570T>C MANE Select	ENSP00000405854.5:p.Asp190=
ENST00000555750.2:c.*408T>C	ENSP00000450980.2:n.*408T>C
ENST00000422005.7:c.*371T>C	ENSP00000411438.4:n.*371T>C
ENST00000438257.8:c.570T>C	ENSP00000405854.4:p.Asp190=
ENST00000555750.1:c.678T>C	ENSP00000450980.1:p.Asp226=
ENST00000555844.1:c.654T>C
ENST00000556811.5:c.546T>C
ENST00000557010.5:c.570T>C	ENSP00000451419.1:p.Asp190=
ENST00000557125.1:c.194T>C	ENSP00000450547.1:n.194T>C
NM_000793.5:c.570T>C	NP_000784.2:p.Asp190=
NM_001007023.3:c.678T>C	NP_001007024.1:p.Asp226=
NM_001242502.1:c.*371T>C	NP_001229431.1:n.*371T>C
NM_001242503.1:c.*371T>C	NP_001229432.1:n.*371T>C
NM_013989.4:c.570T>C	NP_054644.1:p.Asp190=
NM_000793.6:c.570T>C	NP_000784.3:p.Asp190=
NM_001324462.2:c.570T>C	NP_001311391.2:p.Asp190=
NM_001366496.1:c.570T>C	NP_001353425.1:p.Asp190=
NM_013989.5:c.570T>C MANE Select	NP_054644.1:p.Asp190=
NR_158990.1:n.710T>C
NR_158991.1:n.844T>C