LDH info

Canonical Allele Identifier: CA121755
Gene: F11 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 11897
ClinVar RCV Id: RCV000012672
dbSNP Id: rs121965067

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186284167C>A , CM000666.2:g.186284167C>A GRCh38
NC_000004.11:g.187205321C>A , CM000666.1:g.187205321C>A GRCh37
NC_000004.10:g.187442315C>A NCBI36
NG_008051.1:g.23204C>A , LRG_583:g.23204C>A

Transcript Alleles

HGVS Amino-acid change
NM_000128.3:c.1211C>A , LRG_583t1:c.1211C>A NP_000119.1:p.Thr404Asn
XM_005262821.2:c.1214C>A XP_005262878.1:p.Thr405Asn
XM_005262822.2:c.1214C>A XP_005262879.1:p.Thr405Asn
XM_005262823.2:c.944C>A XP_005262880.1:p.Thr315Asn
XM_005262824.1:c.1214C>A XP_005262881.1:p.Thr405Asn
XM_006714137.1:c.1166C>A XP_006714200.1:p.Thr389Asn
XR_938706.1:n.1619C>A
XR_938707.1:n.1619C>A
XM_005262821.4:c.1214C>A XP_005262878.1:p.Thr405Asn
XM_005262822.4:c.1214C>A XP_005262879.1:p.Thr405Asn
XM_005262823.4:c.944C>A XP_005262880.1:p.Thr315Asn
XM_006714137.3:c.1166C>A XP_006714200.1:p.Thr389Asn
XM_017007884.2:c.*2183C>A XP_016863373.1:p.=
XR_001741172.2:n.1685C>A
NM_000128.4:c.1211C>A VV MANE Preferred NP_000119.1:p.Thr404Asn
ENST00000264692.8:c.1049C>A ENSP00000264692.5:p.Thr350Asn
ENST00000403665.6:c.1211C>A ENSP00000384957.2:p.Thr404Asn