LDH info

Canonical Allele Identifier: CA127900
Gene: ALB HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 18196
ClinVar RCV Id: RCV000019840
dbSNP Id: rs75791663

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73415120G>A , CM000666.2:g.73415120G>A GRCh38
NC_000004.11:g.74280837G>A , CM000666.1:g.74280837G>A GRCh37
NC_000004.10:g.74499701G>A NCBI36
NG_009291.1:g.15866G>A

Transcript Alleles

HGVS Amino-acid change
NM_000477.5:c.1144G>A VV NP_000468.1:p.Glu382Lys
NM_000477.6:c.1144G>A VV NP_000468.1:p.Glu382Lys
NM_000477.7:c.1144G>A VV MANE Preferred NP_000468.1:p.Glu382Lys
ENST00000295897.8:c.1144G>A ENSP00000295897.4:p.Glu382Lys
ENST00000401494.7:c.799G>A ENSP00000384695.3:p.Glu267Lys
ENST00000415165.6:c.568G>A ENSP00000401820.2:p.Glu190Lys
ENST00000476441.6:c.*423G>A ENSP00000423727.1:p.=
ENST00000484992.1:n.464G>A
ENST00000503124.5:c.694G>A ENSP00000421027.1:p.Glu232Lys
ENST00000504043.1:n.147G>A
ENST00000505649.5:n.830G>A
ENST00000509063.5:c.1144G>A ENSP00000422784.1:p.Glu382Lys
ENST00000511370.1:n.677G>A
ENST00000621085.4:c.505G>A ENSP00000483421.1:p.Glu169Lys
ENST00000621628.4:c.505G>A ENSP00000480485.1:p.Glu169Lys