LDH info

Canonical Allele Identifier: CA11672411
Gene: F11 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1593

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186274397T>A , CM000666.2:g.186274397T>A GRCh38
NC_000004.11:g.187195551T>A , CM000666.1:g.187195551T>A GRCh37
NC_000004.10:g.187432545T>A NCBI36
NG_008051.1:g.13434T>A , LRG_583:g.13434T>A

Transcript Alleles

HGVS Amino-acid change
NM_000128.3:c.485+122T>A , LRG_583t1:c.485+122T>A NP_000119.1:p.=
XM_005262821.2:c.485+122T>A XP_005262878.1:p.=
XM_005262822.2:c.485+122T>A XP_005262879.1:p.=
XM_005262823.2:c.485+122T>A XP_005262880.1:p.=
XM_005262824.1:c.485+122T>A XP_005262881.1:p.=
XM_006714137.1:c.485+122T>A XP_006714200.1:p.=
XR_938706.1:n.837+122T>A
XR_938707.1:n.837+122T>A
NM_001354804.1:c.*118T>A VV NP_001341733.1:p.=
XM_005262821.4:c.485+122T>A XP_005262878.1:p.=
XM_005262822.4:c.485+122T>A XP_005262879.1:p.=
XM_005262823.4:c.485+122T>A XP_005262880.1:p.=
XM_006714137.3:c.485+122T>A XP_006714200.1:p.=
XM_017007884.2:c.485+122T>A XP_016863373.1:p.=
XM_017007885.2:c.485+122T>A XP_016863374.1:p.=
XM_017007886.2:c.485+122T>A XP_016863375.1:p.=
XR_001741172.2:n.818+122T>A
NM_000128.4:c.485+122T>A VV MANE Preferred NP_000119.1:p.=
NM_001354804.2:c.*118T>A VV NP_001341733.1:p.=
ENST00000264692.8:c.323+1222T>A ENSP00000264692.5:p.=
ENST00000403665.6:c.485+122T>A ENSP00000384957.2:p.=
ENST00000492972.6:c.*118T>A ENSP00000424479.1:p.=
ENST00000514715.1:n.479T>A