Canonical Allele Identifier: CA1167496558
Gene: DIO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53909803T= , CM000663.2:g.53909803T= GRCh38
NC_000001.10:g.54375476T= , CM000663.1:g.54375476T= GRCh37
NC_000001.9:g.54148064T= NCBI36
NG_023306.1:g.20616T=

Transcript Alleles

HGVS Amino-acid change
ENST00000361921.8:c.682-128T= MANE Select ENSP00000354643.4:n.682-128T=
ENST00000322679.10:c.482-128T= ENSP00000323198.6:n.482-128T=
ENST00000361921.7:c.682-128T= ENSP00000354643.3:n.682-128T=
ENST00000388876.3:c.538-128T= ENSP00000373528.3:n.538-128T=
ENST00000524406.5:c.295-128T= ENSP00000434152.1:n.295-128T=
ENST00000525044.5:c.*124-128T= ENSP00000436550.1:n.*124-128T=
ENST00000525202.5:c.490-128T= ENSP00000435725.1:n.490-128T=
ENST00000527060.5:c.*422-128T= ENSP00000435030.1:n.*422-128T=
ENST00000528946.5:c.*60-128T= ENSP00000433891.1:n.*60-128T=
ENST00000529329.1:c.455-128T= ENSP00000432700.1:n.455-128T=
ENST00000530084.5:c.*324-128T= ENSP00000431999.1:n.*324-128T=
ENST00000532493.5:c.338-128T= ENSP00000434758.1:n.338-128T=
ENST00000610607.4:c.*341-128T= ENSP00000483367.1:n.*341-128T=
ENST00000613679.4:c.679-128T= ENSP00000479755.1:n.679-128T=
ENST00000617230.2:c.479-128T= ENSP00000481665.1:n.479-128T=
NM_000792.5:c.682-128T= NP_000783.2:n.682-128T=
NM_001039715.1:c.538-128T= NP_001034804.1:n.538-128T=
NM_001039716.1:c.482-128T= NP_001034805.1:n.482-128T=
NM_213593.3:c.490-128T= NP_998758.1:n.490-128T=
NM_000792.6:c.682-128T= NP_000783.2:n.682-128T=
NM_001039715.2:c.538-128T= NP_001034804.1:n.538-128T=
NM_001039716.2:c.482-128T= NP_001034805.1:n.482-128T=
NM_001324316.1:c.338-128T= NP_001311245.1:n.338-128T=
NM_213593.4:c.490-128T= NP_998758.1:n.490-128T=
NR_136692.1:n.597-128T=
NR_136693.1:n.623-128T=
NM_000792.7:c.682-128T= MANE Select NP_000783.2:n.682-128T=
NM_001039715.3:c.538-128T= NP_001034804.1:n.538-128T=
NM_001039716.3:c.482-128T= NP_001034805.1:n.482-128T=
NM_001324316.2:c.338-128T= NP_001311245.1:n.338-128T=
NM_213593.5:c.490-128T= NP_998758.1:n.490-128T=
NR_136692.2:n.597-128T=
NR_136693.2:n.623-128T=