LDH info

Canonical Allele Identifier: CA16042723
Gene: PTEN HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 372482
dbSNP Id: rs1057517809
COSMIC: COSM5962

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965286G>A , CM000672.2:g.87965286G>A GRCh38
NC_000010.10:g.89725043G>A , CM000672.1:g.89725043G>A GRCh37
NC_000010.9:g.89715023G>A NCBI36
NG_007466.2:g.106848G>A , LRG_311:g.106848G>A

Transcript Alleles

HGVS Amino-acid change
NM_000314.5:c.1027-1G>A VV NP_000305.3:p.=
NM_000314.6:c.1027-1G>A VV NP_000305.3:p.=
NM_001304717.2:c.1546-1G>A VV NP_001291646.2:p.=
NM_001304718.1:c.436-1G>A VV NP_001291647.1:p.=
XM_006717926.2:c.982-1G>A XP_006717989.1:p.=
XM_011539982.1:c.931-1G>A XP_011538284.1:p.=
XR_945791.1:n.1597-1G>A
NM_000314.7:c.1027-1G>A VV NP_000305.3:p.=
NM_001304717.5:c.1546-1G>A VV NP_001291646.4:p.=
NM_001304718.2:c.436-1G>A VV NP_001291647.1:p.=
NM_000314.8:c.1027-1G>A VV MANE Preferred NP_000305.3:p.=
ENST00000371953.7:c.1027-1G>A ENSP00000361021.3:p.=