LDH info

Canonical Allele Identifier: CA257000
Gene:

Identifiers and link-outs to other resources

ClinVar Variation Id: 13884
dbSNP Id: rs121913671

User contributed link-outs

CIViC: CA257000

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116783353G>A , CM000669.2:g.116783353G>A GRCh38
NC_000007.13:g.116423407G>A , CM000669.1:g.116423407G>A GRCh37
NC_000007.12:g.116210643G>A NCBI36
NG_008996.1:g.115949G>A , LRG_662:g.115949G>A

Transcript Alleles

HGVS Amino-acid change
NM_000245.2:c.3682G>A VV NP_000236.2:p.Asp1228Asn
NM_001127500.1:c.3736G>A , LRG_662t1:c.3736G>A NP_001120972.1:p.Asp1246Asn
XM_006715990.2:c.2392G>A XP_006716053.1:p.Asp798Asn
XM_006715991.2:c.2392G>A XP_006716054.1:p.Asp798Asn
XM_011516223.1:c.3739G>A XP_011514525.1:p.Asp1247Asn
NM_000245.3:c.3682G>A VV NP_000236.2:p.Asp1228Asn
NM_001127500.2:c.3736G>A VV NP_001120972.1:p.Asp1246Asn
NM_001324402.1:c.2392G>A VV NP_001311331.1:p.Asp798Asn
XR_001744772.1:n.3813G>A
NM_001127500.3:c.3736G>A VV NP_001120972.1:p.Asp1246Asn
ENST00000318493.10:c.3736G>A ENSP00000317272.6:p.Asp1246Asn
ENST00000397752.7:c.3682G>A ENSP00000380860.3:p.Asp1228Asn