LDH info

Canonical Allele Identifier: CA127912
Gene: ALB HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 18202
ClinVar RCV Id: RCV000019851
dbSNP Id: rs75523493

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73418232G>A , CM000666.2:g.73418232G>A GRCh38
NC_000004.11:g.74283949G>A , CM000666.1:g.74283949G>A GRCh37
NC_000004.10:g.74502813G>A NCBI36
NG_009291.1:g.18978G>A

Transcript Alleles

HGVS Amino-acid change
NM_000477.5:c.1573G>A VV NP_000468.1:p.Glu525Lys
NM_000477.6:c.1573G>A VV NP_000468.1:p.Glu525Lys
NM_000477.7:c.1573G>A VV MANE Preferred NP_000468.1:p.Glu525Lys
ENST00000295897.8:c.1573G>A ENSP00000295897.4:p.Glu525Lys
ENST00000401494.7:c.1228G>A ENSP00000384695.3:p.Glu410Lys
ENST00000415165.6:c.997G>A ENSP00000401820.2:p.Glu333Lys
ENST00000476441.6:c.*852G>A ENSP00000423727.1:p.=
ENST00000486939.1:n.227G>A
ENST00000503124.5:c.1123G>A ENSP00000421027.1:p.Glu375Lys
ENST00000505649.5:n.1120G>A
ENST00000509063.5:c.1573G>A ENSP00000422784.1:p.Glu525Lys
ENST00000511370.1:n.1106G>A
ENST00000621085.4:c.934G>A ENSP00000483421.1:p.Glu312Lys
ENST00000621628.4:c.934G>A ENSP00000480485.1:p.Glu312Lys