LDH info

Canonical Allele Identifier: CA342959
Gene: GLRA1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 38333
ClinVar RCV Id: RCV000031891
dbSNP Id: rs281864920

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151851410A>T , CM000667.2:g.151851410A>T GRCh38
NC_000005.9:g.151230971A>T , CM000667.1:g.151230971A>T GRCh37
NC_000005.8:g.151211164A>T NCBI36
NG_011764.1:g.78427T>A

Transcript Alleles

HGVS Amino-acid change
NM_000171.3:c.892T>A VV NP_000162.2:p.Ser298Thr
NM_001146040.1:c.892T>A VV NP_001139512.1:p.Ser298Thr
NM_001292000.1:c.643T>A VV NP_001278929.1:p.Ser215Thr
XM_005268412.2:c.892T>A XP_005268469.1:p.Ser298Thr
ENST00000274576.8:c.892T>A ENSP00000274576.4:p.Ser298Thr
ENST00000455880.2:c.892T>A ENSP00000411593.2:p.Ser298Thr
ENST00000462581.6:c.*650T>A ENSP00000430595.1:p.=
ENST00000471351.2:n.1175T>A