LDH info

Canonical Allele Identifier: CA16040976
Gene: SLC22A5 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 371182
ClinVar RCV Id: RCV000409176
dbSNP Id: rs1057517069

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132370366G>A , CM000667.2:g.132370366G>A GRCh38
NC_000005.9:g.131706058G>A , CM000667.1:g.131706058G>A GRCh37
NC_000005.8:g.131733957G>A NCBI36
NG_008982.1:g.5658G>A
NG_008982.2:g.5663G>A

Transcript Alleles

HGVS Amino-acid change
NM_001308122.1:c.393+1G>A VV NP_001295051.1:p.=
NM_003060.3:c.393+1G>A VV NP_003051.1:p.=
XR_427718.1:n.662+1G>A
XR_948290.1:n.662+1G>A
XR_948291.1:n.662+1G>A
XM_011543590.2:c.-239+1G>A XP_011541892.1:p.=
XM_017009778.2:c.-32+1G>A XP_016865267.1:p.=
XR_001742215.1:n.662+1G>A
XR_001742216.1:n.662+1G>A
XR_427718.2:n.662+1G>A
XR_948290.2:n.662+1G>A
XR_948291.2:n.662+1G>A
ENST00000245407.7:c.393+1G>A ENSP00000245407.3:p.=
ENST00000415928.5:n.90+1G>A ENSP00000388838.1:p.=
ENST00000435065.6:n.393+1G>A ENSP00000402760.2:p.=
ENST00000437841.6:c.393+1G>A ENSP00000400553.1:p.=