LDH info

Canonical Allele Identifier: CA127939
Gene: ALB HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 18218
ClinVar RCV Id: RCV000019879
dbSNP Id: rs80296402

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73408639G>A , CM000666.2:g.73408639G>A GRCh38
NC_000004.11:g.74274356G>A , CM000666.1:g.74274356G>A GRCh37
NC_000004.10:g.74493220G>A NCBI36
NG_009291.1:g.9385G>A

Transcript Alleles

HGVS Amino-acid change
NM_000477.5:c.316G>A VV NP_000468.1:p.Glu106Lys
NM_000477.6:c.316G>A VV NP_000468.1:p.Glu106Lys
NM_000477.7:c.316G>A VV MANE Preferred NP_000468.1:p.Glu106Lys
ENST00000295897.8:c.316G>A ENSP00000295897.4:p.Glu106Lys
ENST00000401494.7:c.138-716G>A ENSP00000384695.3:p.=
ENST00000415165.6:c.138-3357G>A ENSP00000401820.2:p.=
ENST00000441319.5:n.322G>A ENSP00000392541.1:p.Glu108Lys
ENST00000476441.6:c.80-716G>A ENSP00000423727.1:p.=
ENST00000503124.5:c.33-716G>A ENSP00000421027.1:p.=
ENST00000505649.5:n.2G>A
ENST00000509063.5:c.316G>A ENSP00000422784.1:p.Glu106Lys
ENST00000510166.5:n.352G>A
ENST00000514786.1:n.285G>A
ENST00000515133.5:n.357G>A
ENST00000621085.4:c.316G>A ENSP00000483421.1:p.Glu106Lys
ENST00000621628.4:c.316G>A ENSP00000480485.1:p.Glu106Lys