LDH info

Canonical Allele Identifier: CA392307250
Gene: SLC12A1 HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48229314G>A , CM000677.2:g.48229314G>A GRCh38
NC_000015.9:g.48521511G>A , CM000677.1:g.48521511G>A GRCh37
NC_000015.8:g.46308803G>A NCBI36
NG_021301.1:g.28014G>A

Transcript Alleles

HGVS Amino-acid change
NM_000338.2:c.850G>A VV NP_000329.2:p.Val284Ile
NM_001184832.1:c.850G>A VV NP_001171761.1:p.Val284Ile
XM_005254605.1:c.946G>A XP_005254662.1:p.Val316Ile
XM_005254606.1:c.850G>A XP_005254663.1:p.Val284Ile
XM_006720656.1:c.946G>A XP_006720719.1:p.Val316Ile
XR_931896.1:n.1162G>A
XR_932203.1:n.229+642C>T
XR_932204.1:n.222+642C>T
XM_005254606.2:c.850G>A XP_005254663.1:p.Val284Ile
XR_001751524.2:n.230+642C>T
XR_001751525.1:n.230+642C>T
XR_002957762.1:n.230+642C>T
XR_932204.3:n.224+642C>T
NM_000338.3:c.850G>A VV MANE Preferred NP_000329.2:p.Val284Ile
NM_001184832.2:c.850G>A VV NP_001171761.1:p.Val284Ile
ENST00000330289.10:c.850G>A ENSP00000331550.6:p.Val284Ile
ENST00000380993.7:c.850G>A ENSP00000370381.3:p.Val284Ile
ENST00000396577.7:c.850G>A ENSP00000379822.3:p.Val284Ile
ENST00000558252.5:n.4973G>A
ENST00000558405.5:c.850G>A ENSP00000453409.1:p.Val284Ile
ENST00000559641.5:c.289G>A ENSP00000453230.1:p.Val97Ile
ENST00000559723.2:n.223G>A
ENST00000560692.5:n.4989G>A
ENST00000561127.5:c.289G>A ENSP00000453602.2:p.Val97Ile