LDH info

Canonical Allele Identifier: CA217107
Gene: GFAP HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 16176
dbSNP Id: rs121909718

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44911277C>G , CM000679.2:g.44911277C>G GRCh38
NC_000017.10:g.42988645C>G , CM000679.1:g.42988645C>G GRCh37
NC_000017.9:g.40344171C>G NCBI36
NG_008401.1:g.9270G>C

Transcript Alleles

HGVS Amino-acid change
NM_001131019.2:c.1086G>C VV NP_001124491.1:p.Glu362Asp
NM_001242376.1:c.1086G>C VV NP_001229305.1:p.Glu362Asp
NM_002055.4:c.1086G>C VV NP_002046.1:p.Glu362Asp
NM_001363846.1:c.1086G>C VV NP_001350775.1:p.Glu362Asp
XM_024450690.1:c.1290G>C XP_024306458.1:p.Glu430Asp
XM_024450691.1:c.1290G>C XP_024306459.1:p.Glu430Asp
XM_024450692.1:c.1290G>C XP_024306460.1:p.Glu430Asp
XM_024450693.1:c.1290G>C XP_024306461.1:p.Glu430Asp
NM_002055.5:c.1086G>C VV MANE Preferred NP_002046.1:p.Glu362Asp
NM_001131019.3:c.1086G>C VV NP_001124491.1:p.Glu362Asp
NM_001242376.2:c.1086G>C VV NP_001229305.1:p.Glu362Asp
ENST00000253408.9:c.1086G>C ENSP00000253408.4:p.Glu362Asp
ENST00000435360.6:c.1086G>C ENSP00000403962.1:p.Glu362Asp
ENST00000585543.5:n.239G>C
ENST00000586793.5:c.1086G>C ENSP00000468500.1:p.Glu362Asp
ENST00000587997.5:n.562G>C
ENST00000588640.5:n.466G>C
ENST00000588735.1:c.83-3161G>C ENSP00000466598.1:p.=
ENST00000592320.5:c.663G>C ENSP00000465320.1:p.Glu221Asp