LDH info

Canonical Allele Identifier: CA796592
Gene: SCMH1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs114233776

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.41152625G>A , CM000663.2:g.41152625G>A GRCh38
NC_000001.10:g.41618297G>A , CM000663.1:g.41618297G>A GRCh37
NC_000001.9:g.41390884G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001031694.2:c.50C>T VV NP_001026864.1:p.Pro17Leu
NM_001172218.1:c.-107-941C>T VV NP_001165689.1:p.=
NM_001172219.1:c.107-941C>T VV NP_001165690.1:p.=
NM_001172220.1:c.-37+8250C>T VV NP_001165691.1:p.=
NM_001172221.1:c.-107-941C>T VV NP_001165692.1:p.=
NM_001172222.1:c.6+7100C>T VV NP_001165693.1:p.=
NM_012236.3:c.6+7100C>T VV NP_036368.1:p.=
XM_006710462.2:c.107-941C>T XP_006710525.1:p.=
XM_006710464.1:c.-107-941C>T XP_006710527.1:p.=
XM_006710469.2:c.107-941C>T XP_006710532.1:p.=
XM_006710470.2:c.107-941C>T XP_006710533.1:p.=
XM_011541032.1:c.107-941C>T XP_011539334.1:p.=
XM_011541033.1:c.50C>T XP_011539335.1:p.Pro17Leu
XM_011541034.1:c.107-941C>T XP_011539336.1:p.=
XM_011541035.1:c.6+7100C>T XP_011539337.1:p.=
XM_011541036.1:c.-107-941C>T XP_011539338.1:p.=
XM_011541037.1:c.-37+8250C>T XP_011539339.1:p.=
XM_011541038.1:c.107-941C>T XP_011539340.1:p.=
XM_011541039.1:c.107-941C>T XP_011539341.1:p.=
XM_011541040.1:c.107-941C>T XP_011539342.1:p.=
XM_011541041.1:c.107-941C>T XP_011539343.1:p.=
XM_011541042.1:c.107-941C>T XP_011539344.1:p.=
XM_011541043.1:c.-459-941C>T XP_011539345.1:p.=
XR_426594.2:n.309-941C>T
XR_426595.2:n.309-941C>T
XR_946584.1:n.309-941C>T
XR_946585.1:n.309-941C>T
XR_946586.1:n.261C>T
XR_946587.1:n.309-941C>T
NM_001172222.2:c.6+7100C>T VV NP_001165693.1:p.=
NM_001350667.1:c.-201-941C>T VV NP_001337596.1:p.=
NM_001350668.1:c.-455-941C>T VV NP_001337597.1:p.=
NR_135092.1:n.419C>T
XM_011541032.2:c.107-941C>T XP_011539334.1:p.=
XM_011541033.2:c.50C>T XP_011539335.1:p.Pro17Leu
XM_011541035.2:c.6+7100C>T XP_011539337.1:p.=
XM_011541036.2:c.-107-941C>T XP_011539338.1:p.=
XM_011541040.2:c.107-941C>T XP_011539342.1:p.=
XM_011541043.2:c.-459-941C>T XP_011539345.1:p.=
XM_017000698.1:c.-11C>T XP_016856187.1:p.=
XM_017000699.1:c.-37+8250C>T XP_016856188.1:p.=
XM_017000700.1:c.6+7100C>T XP_016856189.1:p.=
XM_017000702.1:c.-201-941C>T XP_016856191.1:p.=
XM_017000703.1:c.-131+7100C>T XP_016856192.1:p.=
XM_017000708.1:c.-107-941C>T XP_016856197.1:p.=
XM_017000711.1:c.-107-941C>T XP_016856200.1:p.=
XM_017000712.1:c.-37+8250C>T XP_016856201.1:p.=
XM_017000713.2:c.-131+8250C>T XP_016856202.1:p.=
XM_024454203.1:c.-228C>T XP_024309971.1:p.=
XM_024454204.1:c.-201-941C>T XP_024309972.1:p.=
XM_024454206.1:c.-131+7100C>T XP_024309974.1:p.=
XR_001737045.1:n.309-941C>T
XR_001737046.1:n.309-941C>T
XR_001737051.1:n.309-941C>T
XR_001737052.1:n.258-941C>T
XR_001737053.1:n.527+7100C>T
XR_001737054.1:n.258-941C>T
XR_002959757.1:n.309-941C>T
XR_002959760.1:n.309-941C>T
XR_002959761.1:n.309-941C>T
XR_002959762.1:n.309-941C>T
XR_002959763.1:n.309-941C>T
XR_946584.2:n.309-941C>T
NM_001172218.2:c.-107-941C>T VV NP_001165689.1:p.=
NM_001172219.2:c.107-941C>T VV NP_001165690.1:p.=
NM_001172220.2:c.-37+8250C>T VV NP_001165691.1:p.=
NM_001350667.2:c.-201-941C>T VV NP_001337596.1:p.=
NM_012236.4:c.6+7100C>T VV NP_036368.1:p.=
ENST00000326197.11:c.50C>T ENSP00000318094.7:p.Pro17Leu
ENST00000337495.9:c.107-941C>T ENSP00000337352.5:p.=
ENST00000361191.9:c.-37+8250C>T ENSP00000354656.5:p.=
ENST00000361705.7:c.6+7100C>T ENSP00000354996.3:p.=
ENST00000372595.5:c.-107-941C>T ENSP00000361676.1:p.=
ENST00000372596.5:c.-107-941C>T ENSP00000361677.1:p.=
ENST00000372597.5:c.6+7100C>T ENSP00000361678.1:p.=
ENST00000397171.6:c.-107-941C>T ENSP00000380356.2:p.=
ENST00000397174.6:n.50C>T ENSP00000380359.3:p.Pro17Leu
ENST00000402904.6:c.-107-941C>T ENSP00000386079.3:p.=
ENST00000456518.3:c.6+7100C>T ENSP00000403974.2:p.=