LDH info

Canonical Allele Identifier: CA490016149
Gene: SLC12A1 HGNC NCBI

Identifiers and link-outs to other resources

MyVariant Identifiers: chr15:g.48521507T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48229310T>C , CM000677.2:g.48229310T>C GRCh38
NC_000015.9:g.48521507T>C , CM000677.1:g.48521507T>C GRCh37
NC_000015.8:g.46308799T>C NCBI36
NG_021301.1:g.28010T>C

Transcript Alleles

HGVS Amino-acid change
NM_000338.2:c.846T>C VV NP_000329.2:p.Thr282=
NM_001184832.1:c.846T>C VV NP_001171761.1:p.Thr282=
XM_005254605.1:c.942T>C XP_005254662.1:p.Thr314=
XM_005254606.1:c.846T>C XP_005254663.1:p.Thr282=
XM_006720656.1:c.942T>C XP_006720719.1:p.Thr314=
XR_931896.1:n.1158T>C
XR_932203.1:n.229+646A>G
XR_932204.1:n.222+646A>G
XM_005254606.2:c.846T>C XP_005254663.1:p.Thr282=
XR_001751524.2:n.230+646A>G
XR_001751525.1:n.230+646A>G
XR_002957762.1:n.230+646A>G
XR_932204.3:n.224+646A>G
NM_000338.3:c.846T>C VV MANE Preferred NP_000329.2:p.Thr282=
NM_001184832.2:c.846T>C VV NP_001171761.1:p.Thr282=
ENST00000330289.10:c.846T>C ENSP00000331550.6:p.Thr282=
ENST00000380993.7:c.846T>C ENSP00000370381.3:p.Thr282=
ENST00000396577.7:c.846T>C ENSP00000379822.3:p.Thr282=
ENST00000558252.5:n.4969T>C
ENST00000558405.5:c.846T>C ENSP00000453409.1:p.Thr282=
ENST00000559641.5:c.285T>C ENSP00000453230.1:p.Thr95=
ENST00000559723.2:n.219T>C
ENST00000560692.5:n.4985T>C
ENST00000561127.5:c.285T>C ENSP00000453602.2:p.Thr95=