LDH info

Canonical Allele Identifier: CA199086

Identifiers and link-outs to other resources

ClinVar Variation Id: 188887
dbSNP Id: rs201007090

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186286490G>A , CM000666.2:g.186286490G>A GRCh38
NC_000004.11:g.187207644G>A , CM000666.1:g.187207644G>A GRCh37
NC_000004.10:g.187444638G>A NCBI36
NG_008051.1:g.25527G>A , LRG_583:g.25527G>A

Transcript Alleles

HGVS Amino-acid change
NM_000128.3:c.1556G>A , LRG_583t1:c.1556G>A (F11) NP_000119.1:p.Trp519Ter
NR_033900.1:n.1067-224C>T (F11-AS1)
XM_005262821.2:c.1559G>A (F11) XP_005262878.1:p.Trp520Ter
XM_005262822.2:c.1483+677G>A (F11) XP_005262879.1:p.=
XM_005262823.2:c.1289G>A (F11) XP_005262880.1:p.Trp430Ter
XM_005262824.1:c.1484-56G>A (F11) XP_005262881.1:p.=
XM_006714137.1:c.1511G>A (F11) XP_006714200.1:p.Trp504Ter
XR_938706.1:n.1964G>A (F11)
XR_938707.1:n.1888+677G>A (F11)
XM_005262821.4:c.1559G>A (F11) XP_005262878.1:p.Trp520Ter
XM_005262822.4:c.1483+677G>A (F11) XP_005262879.1:p.=
XM_005262823.4:c.1289G>A (F11) XP_005262880.1:p.Trp430Ter
XM_006714137.3:c.1511G>A (F11) XP_006714200.1:p.Trp504Ter
XR_001741172.2:n.2030G>A (F11)
NM_000128.4:c.1556G>A (F11) VV NP_000119.1:p.Trp519Ter
ENST00000264691.4:n.176+677G>A
ENST00000264692.8:c.1394G>A ENSP00000264692.5:p.Trp465Ter
ENST00000403665.6:c.1556G>A ENSP00000384957.2:p.Trp519Ter