LDH info

Canonical Allele Identifier: CA10272847
Gene: TSPO HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs6971

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43162920A>G , CM000684.2:g.43162920A>G GRCh38
NC_000022.10:g.43558926A>G , CM000684.1:g.43558926A>G GRCh37
NC_000022.9:g.41888870A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_000714.5:c.439A>G VV NP_000705.2:p.Thr147Ala
NM_001256530.1:c.439A>G VV NP_001243459.1:p.Thr147Ala
NM_001256531.1:c.439A>G VV NP_001243460.1:p.Thr147Ala
NR_046308.1:n.348A>G
NM_000714.6:c.439A>G VV MANE Preferred NP_000705.2:p.Thr147Ala
NR_046308.2:n.303A>G
ENST00000329563.8:c.439A>G ENSP00000328973.4:p.Thr147Ala
ENST00000337554.7:c.439A>G ENSP00000338004.3:p.Thr147Ala
ENST00000396265.4:c.439A>G ENSP00000379563.4:p.Thr147Ala
ENST00000583777.5:c.127A>G ENSP00000463495.1:p.Thr43Ala