LDH info

Canonical Allele Identifier: CA150790
Gene: PLD3 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 120224
ClinVar RCV Id: RCV000106322
dbSNP Id: rs145999145

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40371688G>A , CM000681.2:g.40371688G>A GRCh38
NC_000019.9:g.40877595G>A , CM000681.1:g.40877595G>A GRCh37
NC_000019.8:g.45569435G>A NCBI36
NG_034098.1:g.28264G>A

Transcript Alleles

HGVS Amino-acid change
NM_001031696.3:c.694G>A VV NP_001026866.1:p.Val232Met
NM_001291311.1:c.694G>A VV NP_001278240.1:p.Val232Met
NM_012268.3:c.694G>A VV NP_036400.2:p.Val232Met
XM_005258704.1:c.694G>A XP_005258761.1:p.Val232Met
XM_005258705.2:c.694G>A XP_005258762.1:p.Val232Met
XM_005258707.3:c.694G>A XP_005258764.1:p.Val232Met
XM_005258708.2:c.694G>A XP_005258765.1:p.Val232Met
XM_005258709.3:c.694G>A XP_005258766.1:p.Val232Met
XM_005258710.3:c.694G>A XP_005258767.1:p.Val232Met
XM_006723122.1:c.694G>A XP_006723185.1:p.Val232Met
XM_011526692.1:c.694G>A XP_011524994.1:p.Val232Met
XM_011526693.1:c.694G>A XP_011524995.1:p.Val232Met
XM_005258704.2:c.694G>A XP_005258761.1:p.Val232Met
XM_005258707.4:c.694G>A XP_005258764.1:p.Val232Met
XM_005258708.4:c.694G>A XP_005258765.1:p.Val232Met
XM_005258709.4:c.694G>A XP_005258766.1:p.Val232Met
XM_005258710.5:c.694G>A XP_005258767.1:p.Val232Met
XM_017026546.1:c.694G>A XP_016882035.1:p.Val232Met
XM_017026548.1:c.694G>A XP_016882037.1:p.Val232Met
XM_017026549.1:c.694G>A XP_016882038.1:p.Val232Met
XM_024451438.1:c.694G>A XP_024307206.1:p.Val232Met
NM_012268.4:c.694G>A VV MANE Preferred NP_036400.2:p.Val232Met
ENST00000356508.9:c.694G>A ENSP00000348901.5:p.Val232Met
ENST00000409281.5:c.694G>A ENSP00000387022.1:p.Val232Met
ENST00000409419.5:c.694G>A ENSP00000386293.1:p.Val232Met
ENST00000409587.5:c.694G>A ENSP00000387050.1:p.Val232Met
ENST00000409735.8:c.694G>A ENSP00000386938.3:p.Val232Met
ENST00000475983.1:n.212G>A
ENST00000492243.1:n.580G>A