LDH info

Canonical Allele Identifier: CA000330
Gene: PTEN HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 7841
dbSNP Id: rs121909236

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87925529C>G , CM000672.2:g.87925529C>G GRCh38
NC_000010.10:g.89685286C>G , CM000672.1:g.89685286C>G GRCh37
NC_000010.9:g.89675266C>G NCBI36
NG_007466.2:g.67091C>G , LRG_311:g.67091C>G

Transcript Alleles

HGVS Amino-acid change
NM_000314.5:c.181C>G VV NP_000305.3:p.His61Asp
NM_000314.6:c.181C>G VV NP_000305.3:p.His61Asp
NM_001304717.2:c.700C>G VV NP_001291646.2:p.His234Asp
NM_001304718.1:c.-541-5517C>G VV NP_001291647.1:p.=
XM_006717926.2:c.165-5517C>G XP_006717989.1:p.=
XM_011539981.1:c.181C>G XP_011538283.1:p.His61Asp
XM_011539982.1:c.85C>G XP_011538284.1:p.His29Asp
XR_945789.1:n.893C>G
XR_945790.1:n.893C>G
XR_945791.1:n.893C>G
NM_000314.7:c.181C>G VV NP_000305.3:p.His61Asp
NM_001304717.5:c.700C>G VV NP_001291646.4:p.His234Asp
NM_001304718.2:c.-541-5517C>G VV NP_001291647.1:p.=
ENST00000371953.7:c.181C>G ENSP00000361021.3:p.His61Asp
ENST00000498703.1:n.7C>G
ENST00000610634.1:c.79C>G ENSP00000477517.1:p.His27Asp