LDH info

Canonical Allele Identifier: CA392306867
Gene: SLC12A1 HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48229222G>T , CM000677.2:g.48229222G>T GRCh38
NC_000015.9:g.48521419G>T , CM000677.1:g.48521419G>T GRCh37
NC_000015.8:g.46308711G>T NCBI36
NG_021301.1:g.27922G>T

Transcript Alleles

HGVS Amino-acid change
NM_000338.2:c.758G>T VV NP_000329.2:p.Gly253Val
NM_001184832.1:c.758G>T VV NP_001171761.1:p.Gly253Val
XM_005254605.1:c.854G>T XP_005254662.1:p.Gly285Val
XM_005254606.1:c.758G>T XP_005254663.1:p.Gly253Val
XM_006720656.1:c.854G>T XP_006720719.1:p.Gly285Val
XR_931896.1:n.1070G>T
XR_932203.1:n.229+734C>A
XR_932204.1:n.222+734C>A
XM_005254606.2:c.758G>T XP_005254663.1:p.Gly253Val
XR_001751524.2:n.230+734C>A
XR_001751525.1:n.230+734C>A
XR_002957762.1:n.230+734C>A
XR_932204.3:n.224+734C>A
NM_000338.3:c.758G>T VV MANE Preferred NP_000329.2:p.Gly253Val
NM_001184832.2:c.758G>T VV NP_001171761.1:p.Gly253Val
ENST00000330289.10:c.758G>T ENSP00000331550.6:p.Gly253Val
ENST00000380993.7:c.758G>T ENSP00000370381.3:p.Gly253Val
ENST00000396577.7:c.758G>T ENSP00000379822.3:p.Gly253Val
ENST00000558252.5:n.4881G>T
ENST00000558405.5:c.758G>T ENSP00000453409.1:p.Gly253Val
ENST00000559641.5:c.197G>T ENSP00000453230.1:p.Gly66Val
ENST00000559723.2:n.131G>T
ENST00000560692.5:n.4897G>T
ENST00000561127.5:c.197G>T ENSP00000453602.2:p.Gly66Val