LDH info

Canonical Allele Identifier: CA257213
Gene: MPI HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 14349
ClinVar RCV Id: RCV000015423
dbSNP Id: rs28928906

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74897050G>A , CM000677.2:g.74897050G>A GRCh38
NC_000015.9:g.75189391G>A , CM000677.1:g.75189391G>A GRCh37
NC_000015.8:g.72976444G>A NCBI36
NG_008921.1:g.11982G>A

Transcript Alleles

HGVS Amino-acid change
NM_001289155.1:c.845-462G>A VV NP_001276084.1:p.=
NM_001289156.1:c.734G>A VV NP_001276085.1:p.Arg245His
NM_001289157.1:c.701G>A VV NP_001276086.1:p.Arg234His
NM_002435.2:c.884G>A VV NP_002426.1:p.Arg295His
XM_011521592.1:c.872G>A XP_011519894.1:p.Arg291His
XM_011521593.1:c.824G>A XP_011519895.1:p.Arg275His
NM_001330372.1:c.824G>A VV NP_001317301.1:p.Arg275His
XM_017022208.1:c.785-462G>A XP_016877697.1:p.=
XM_017022209.2:c.695-462G>A XP_016877698.1:p.=
NM_002435.3:c.884G>A VV MANE Preferred NP_002426.1:p.Arg295His
NM_001289155.2:c.845-462G>A VV NP_001276084.1:p.=
NM_001289156.2:c.734G>A VV NP_001276085.1:p.Arg245His
NM_001289157.2:c.701G>A VV NP_001276086.1:p.Arg234His
NM_001330372.2:c.824G>A VV NP_001317301.1:p.Arg275His
ENST00000323744.10:c.701G>A ENSP00000318192.6:p.Arg234His
ENST00000352410.8:c.884G>A ENSP00000318318.6:p.Arg295His
ENST00000535694.5:c.734G>A ENSP00000440447.1:p.Arg245His
ENST00000562800.5:c.256-489G>A ENSP00000457619.1:p.=
ENST00000563786.5:c.824G>A ENSP00000455241.1:p.Arg275His
ENST00000566377.5:c.845-462G>A ENSP00000455405.1:p.=
ENST00000566556.1:n.1617G>A
ENST00000567177.1:n.623-462G>A ENSP00000457013.1:p.=
ENST00000569931.5:c.824G>A ENSP00000455161.1:p.Arg275His