LDH info

Canonical Allele Identifier: CA16041817
Gene: ALDH3A2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 370452
ClinVar RCV Id: RCV000411369

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.19664947G>C , CM000679.2:g.19664947G>C GRCh38
NC_000017.10:g.19568260G>C , CM000679.1:g.19568260G>C GRCh37
NC_000017.9:g.19508852G>C NCBI36
NG_007095.2:g.21197G>C

Transcript Alleles

HGVS Amino-acid change
NM_000382.2:c.1108-1G>C VV NP_000373.1:p.=
NM_001031806.1:c.1108-1G>C VV NP_001026976.1:p.=
XM_011523732.1:c.1108-1G>C XP_011522034.1:p.=
XM_011523733.1:c.1108-1G>C XP_011522035.1:p.=
XM_011523733.2:c.1108-1G>C XP_011522035.1:p.=
XM_017024355.1:c.1108-1G>C XP_016879844.1:p.=
XM_017024356.2:c.1108-1G>C XP_016879845.1:p.=
XM_017024357.1:c.1108-1G>C XP_016879846.1:p.=
XM_017024358.2:c.1108-1G>C XP_016879847.1:p.=
XM_024450651.1:c.529-1G>C XP_024306419.1:p.=
XM_024450652.1:c.529-1G>C XP_024306420.1:p.=
NM_000382.3:c.1108-1G>C VV NP_000373.1:p.=
NM_001031806.2:c.1108-1G>C VV NP_001026976.1:p.=
NM_001369136.1:c.1108-1G>C VV NP_001356065.1:p.=
NM_001369137.1:c.1108-1G>C VV NP_001356066.1:p.=
NM_001369138.1:c.1108-1G>C VV NP_001356067.1:p.=
NM_001369139.1:c.1108-1G>C VV NP_001356068.1:p.=
NM_001369146.1:c.1108-1G>C VV NP_001356075.1:p.=
NM_001369148.1:c.529-1G>C VV NP_001356077.1:p.=
ENST00000176643.10:c.1108-1G>C ENSP00000176643.6:p.=
ENST00000339618.8:c.1108-1G>C ENSP00000345774.4:p.=
ENST00000395575.6:c.1108-1G>C ENSP00000378942.2:p.=
ENST00000472059.5:c.*666-1G>C ENSP00000458397.1:p.=
ENST00000476965.5:n.858-1G>C
ENST00000571163.1:n.127-1G>C ENSP00000459977.1:p.=
ENST00000573947.1:n.114+1448G>C ENSP00000462933.1:p.=
ENST00000579855.5:c.1108-1G>C ENSP00000463637.1:p.=
ENST00000581518.5:c.1108-1G>C ENSP00000461916.1:p.=
ENST00000582991.5:c.1107+1448G>C ENSP00000464153.1:p.=
ENST00000630662.2:c.127-1G>C ENSP00000487353.1:p.=
ENST00000631291.2:c.1107+1448G>C ENSP00000486085.1:p.=