Canonical Allele Identifier: CA390764988

Gene: DIO2

Linked Data

• MyVariant Identifiers: chr14:g.80669390T>C (hg19) ; chr14:g.80203047T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.80203047T>C , CM000676.2:g.80203047T>C	GRCh38
NC_000014.8:g.80669390T>C , CM000676.1:g.80669390T>C	GRCh37
NC_000014.7:g.79739143T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000438257.9:c.464A>G MANE Select	ENSP00000405854.5:p.Asp155Gly
ENST00000555750.2:c.*302A>G	ENSP00000450980.2:n.*302A>G
ENST00000422005.7:c.*265A>G	ENSP00000411438.4:n.*265A>G
ENST00000438257.8:c.464A>G	ENSP00000405854.4:p.Asp155Gly
ENST00000555750.1:c.572A>G	ENSP00000450980.1:p.Asp191Gly
ENST00000555844.1:c.548A>G
ENST00000556811.5:c.440A>G
ENST00000557010.5:c.464A>G	ENSP00000451419.1:p.Asp155Gly
ENST00000557125.1:c.88A>G	ENSP00000450547.1:p.Thr30Ala
NM_000793.5:c.464A>G	NP_000784.2:p.Asp155Gly
NM_001007023.3:c.572A>G	NP_001007024.1:p.Asp191Gly
NM_001242502.1:c.*265A>G	NP_001229431.1:n.*265A>G
NM_001242503.1:c.*265A>G	NP_001229432.1:n.*265A>G
NM_013989.4:c.464A>G	NP_054644.1:p.Asp155Gly
NM_000793.6:c.464A>G	NP_000784.3:p.Asp155Gly
NM_001324462.2:c.464A>G	NP_001311391.2:p.Asp155Gly
NM_001366496.1:c.464A>G	NP_001353425.1:p.Asp155Gly
NM_013989.5:c.464A>G MANE Select	NP_054644.1:p.Asp155Gly
NR_158990.1:n.604A>G
NR_158991.1:n.738A>G