LDH info

Canonical Allele Identifier: CA121759
Gene: F11 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 11899
ClinVar RCV Id: RCV000012674
dbSNP Id: rs121965068

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186284245C>T , CM000666.2:g.186284245C>T GRCh38
NC_000004.11:g.187205399C>T , CM000666.1:g.187205399C>T GRCh37
NC_000004.10:g.187442393C>T NCBI36
NG_008051.1:g.23282C>T , LRG_583:g.23282C>T

Transcript Alleles

HGVS Amino-acid change
NM_000128.3:c.1289C>T , LRG_583t1:c.1289C>T NP_000119.1:p.Ala430Val
XM_005262821.2:c.1292C>T XP_005262878.1:p.Ala431Val
XM_005262822.2:c.1292C>T XP_005262879.1:p.Ala431Val
XM_005262823.2:c.1022C>T XP_005262880.1:p.Ala341Val
XM_005262824.1:c.1292C>T XP_005262881.1:p.Ala431Val
XM_006714137.1:c.1244C>T XP_006714200.1:p.Ala415Val
XR_938706.1:n.1697C>T
XR_938707.1:n.1697C>T
XM_005262821.4:c.1292C>T XP_005262878.1:p.Ala431Val
XM_005262822.4:c.1292C>T XP_005262879.1:p.Ala431Val
XM_005262823.4:c.1022C>T XP_005262880.1:p.Ala341Val
XM_006714137.3:c.1244C>T XP_006714200.1:p.Ala415Val
XR_001741172.2:n.1763C>T
NM_000128.4:c.1289C>T VV MANE Preferred NP_000119.1:p.Ala430Val
ENST00000264692.8:c.1127C>T ENSP00000264692.5:p.Ala376Val
ENST00000403665.6:c.1289C>T ENSP00000384957.2:p.Ala430Val