LDH info

Canonical Allele Identifier: CA7292659
Gene: DIO2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs225014

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.80203237T>C , CM000676.2:g.80203237T>C GRCh38
NC_000014.8:g.80669580T>C , CM000676.1:g.80669580T>C GRCh37
NC_000014.7:g.79739333T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_000793.5:c.274A>G VV NP_000784.2:p.Thr92Ala
NM_001007023.3:c.382A>G VV NP_001007024.1:p.Thr128Ala
NM_001242502.1:c.*75A>G VV NP_001229431.1:p.=
NM_001242503.1:c.*75A>G VV NP_001229432.1:p.=
NM_013989.4:c.274A>G VV NP_054644.1:p.Thr92Ala
NM_000793.6:c.274A>G VV NP_000784.3:p.Thr92Ala
NM_001324462.2:c.274A>G VV NP_001311391.2:p.Thr92Ala
NM_001366496.1:c.274A>G VV NP_001353425.1:p.Thr92Ala
NM_013989.5:c.274A>G VV MANE Preferred NP_054644.1:p.Thr92Ala
NR_158990.1:n.414A>G
NR_158991.1:n.548A>G
ENST00000422005.7:c.*75A>G ENSP00000411438.4:p.=
ENST00000438257.8:c.274A>G ENSP00000405854.4:p.Thr92Ala
ENST00000555750.1:c.382A>G ENSP00000450980.1:p.Thr128Ala
ENST00000555844.1:n.358A>G
ENST00000556811.5:n.250A>G
ENST00000557010.5:c.274A>G ENSP00000451419.1:p.Thr92Ala
ENST00000557125.1:n.49-151A>G ENSP00000450547.1:p.=