LDH info

Canonical Allele Identifier: CA258995281
Gene: NUBPL HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs7142881

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.31624342G>A , CM000676.2:g.31624342G>A GRCh38
NC_000014.8:g.32093548G>A , CM000676.1:g.32093548G>A GRCh37
NC_000014.7:g.31163299G>A NCBI36
NG_028349.1:g.67958G>A

Transcript Alleles

HGVS Amino-acid change
NM_001201573.1:c.94+24963G>A VV NP_001188502.1:p.=
NM_025152.2:c.382+24963G>A VV NP_079428.2:p.=
NR_120408.1:n.437+24963G>A
XM_005268099.3:c.382+24963G>A XP_005268156.1:p.=
XM_011537181.1:c.107+24963G>A XP_011535483.1:p.=
XM_011537182.1:c.-74+24963G>A XP_011535484.1:p.=
XM_011537183.1:c.382+24963G>A XP_011535485.1:p.=
XM_011537181.2:c.107+24963G>A XP_011535483.1:p.=
XM_011537182.2:c.-74+24963G>A XP_011535484.1:p.=
XM_011537183.2:c.382+24963G>A XP_011535485.1:p.=
XM_017021664.1:c.382+24963G>A XP_016877153.1:p.=
XM_017021665.2:c.382+24963G>A XP_016877154.1:p.=
XM_017021666.1:c.382+24963G>A XP_016877155.1:p.=
XM_017021667.1:c.-2+24963G>A XP_016877156.1:p.=
NM_025152.3:c.382+24963G>A VV MANE Preferred NP_079428.2:p.=
NR_120408.2:n.418+24963G>A
ENST00000281081.11:c.382+24963G>A ENSP00000281081.7:p.=
ENST00000547839.5:c.382+24963G>A ENSP00000449918.1:p.=
ENST00000548937.5:n.386+24963G>A
ENST00000549838.5:n.346+24963G>A ENSP00000447658.1:p.=
ENST00000550355.1:n.331+24963G>A
ENST00000550649.5:c.291+59294G>A ENSP00000447618.1:p.=
ENST00000551314.1:c.226+24963G>A ENSP00000447234.1:p.=
ENST00000552489.5:n.476+24963G>A ENSP00000447316.1:p.=