LDH info

Canonical Allele Identifier: CA15371762
Gene: NPR3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10061804

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.32748531G>A , CM000667.2:g.32748531G>A GRCh38
NC_000005.9:g.32748637G>A , CM000667.1:g.32748637G>A GRCh37
NC_000005.8:g.32784394G>A NCBI36
NG_028162.1:g.42895G>A
NG_028162.2:g.64456G>A

Transcript Alleles

HGVS Amino-acid change
NM_000908.3:c.1059+9501G>A VV NP_000899.1:p.=
NM_001204375.1:c.1059+9501G>A VV NP_001191304.1:p.=
NM_001204376.1:c.411+9501G>A VV NP_001191305.1:p.=
XM_005248309.1:c.411+9501G>A XP_005248366.1:p.=
XM_011514047.1:c.390+9501G>A XP_011512349.1:p.=
XM_011514048.1:c.339+9501G>A XP_011512350.1:p.=
XM_011514049.1:c.282+9501G>A XP_011512351.1:p.=
NM_001363652.1:c.411+9501G>A VV NP_001350581.1:p.=
NM_001364458.1:c.339+9501G>A VV NP_001351387.1:p.=
NM_001364460.1:c.288+9501G>A VV NP_001351389.1:p.=
XM_011514047.2:c.390+9501G>A XP_011512349.1:p.=
XM_011514049.3:c.282+9501G>A XP_011512351.1:p.=
XM_017009492.2:c.936+9501G>A XP_016864981.1:p.=
NM_001204375.2:c.1059+9501G>A VV MANE Preferred NP_001191304.1:p.=
NM_000908.4:c.1059+9501G>A VV NP_000899.1:p.=
NM_001363652.2:c.411+9501G>A VV NP_001350581.1:p.=
NM_001364458.2:c.339+9501G>A VV NP_001351387.1:p.=
NM_001364460.2:c.288+9501G>A VV NP_001351389.1:p.=
ENST00000265074.12:c.1059+9501G>A ENSP00000265074.8:p.=
ENST00000326958.5:c.411+9501G>A ENSP00000318340.2:p.=
ENST00000415167.2:c.1059+9501G>A ENSP00000398028.2:p.=
ENST00000434067.6:c.411+9501G>A ENSP00000388408.2:p.=
ENST00000506712.1:n.420+9501G>A
ENST00000509104.5:c.390+9501G>A ENSP00000425325.1:p.=