LDH info

Canonical Allele Identifier: CA12737097
Gene: SLC30A8 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11989843

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117138754A>G , CM000670.2:g.117138754A>G GRCh38
NC_000008.10:g.118150993A>G , CM000670.1:g.118150993A>G GRCh37
NC_000008.9:g.118220174A>G NCBI36
NG_016991.1:g.193482A>G

Transcript Alleles

HGVS Amino-acid change
NM_001172811.1:c.-106-8065A>G VV NP_001166282.1:p.=
NM_001172813.1:c.-107+3356A>G VV NP_001166284.1:p.=
NM_001172814.1:c.-107+3356A>G VV NP_001166285.1:p.=
NM_001172815.1:c.-107+3356A>G VV NP_001166286.1:p.=
NM_173851.2:c.71+3356A>G VV NP_776250.2:p.=
XM_011516881.1:c.71+3356A>G XP_011515183.1:p.=
XR_928569.1:n.1020+33861T>C
XR_928570.1:n.1021-20968T>C
NM_001172815.2:c.-107+3356A>G VV NP_001166286.1:p.=
XM_024447083.1:c.-106-8065A>G XP_024302851.1:p.=
XR_928569.2:n.973+33861T>C
XR_928570.2:n.974-20968T>C
NM_001172811.2:c.-106-8065A>G VV NP_001166282.1:p.=
NM_001172813.2:c.-107+3356A>G VV NP_001166284.1:p.=
NM_001172814.2:c.-107+3356A>G VV NP_001166285.1:p.=
NM_173851.3:c.71+3356A>G VV NP_776250.2:p.=
ENST00000427715.2:c.-107+3356A>G ENSP00000407505.2:p.=
ENST00000456015.6:n.71+3356A>G ENSP00000415011.2:p.=
ENST00000518396.5:c.-107+3356A>G ENSP00000485167.1:p.=
ENST00000518521.5:c.-77+3356A>G ENSP00000485566.1:p.=
ENST00000519688.5:c.-107+3356A>G ENSP00000431069.1:p.=
ENST00000520469.1:n.325+3356A>G
ENST00000521035.5:n.461+3356A>G
ENST00000521243.5:c.-106-8065A>G ENSP00000428545.1:p.=
ENST00000524274.5:c.-106-8065A>G ENSP00000427760.1:p.=