LDH info

Canonical Allele Identifier: CA392307231
Gene: SLC12A1 HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48229308A>T , CM000677.2:g.48229308A>T GRCh38
NC_000015.9:g.48521505A>T , CM000677.1:g.48521505A>T GRCh37
NC_000015.8:g.46308797A>T NCBI36
NG_021301.1:g.28008A>T

Transcript Alleles

HGVS Amino-acid change
NM_000338.2:c.844A>T VV NP_000329.2:p.Thr282Ser
NM_001184832.1:c.844A>T VV NP_001171761.1:p.Thr282Ser
XM_005254605.1:c.940A>T XP_005254662.1:p.Thr314Ser
XM_005254606.1:c.844A>T XP_005254663.1:p.Thr282Ser
XM_006720656.1:c.940A>T XP_006720719.1:p.Thr314Ser
XR_931896.1:n.1156A>T
XR_932203.1:n.229+648T>A
XR_932204.1:n.222+648T>A
XM_005254606.2:c.844A>T XP_005254663.1:p.Thr282Ser
XR_001751524.2:n.230+648T>A
XR_001751525.1:n.230+648T>A
XR_002957762.1:n.230+648T>A
XR_932204.3:n.224+648T>A
NM_000338.3:c.844A>T VV MANE Preferred NP_000329.2:p.Thr282Ser
NM_001184832.2:c.844A>T VV NP_001171761.1:p.Thr282Ser
ENST00000330289.10:c.844A>T ENSP00000331550.6:p.Thr282Ser
ENST00000380993.7:c.844A>T ENSP00000370381.3:p.Thr282Ser
ENST00000396577.7:c.844A>T ENSP00000379822.3:p.Thr282Ser
ENST00000558252.5:n.4967A>T
ENST00000558405.5:c.844A>T ENSP00000453409.1:p.Thr282Ser
ENST00000559641.5:c.283A>T ENSP00000453230.1:p.Thr95Ser
ENST00000559723.2:n.217A>T
ENST00000560692.5:n.4983A>T
ENST00000561127.5:c.283A>T ENSP00000453602.2:p.Thr95Ser