LDH info

Canonical Allele Identifier: CA16040977
Gene: SLC22A5 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 371227
ClinVar RCV Id: RCV000410584
dbSNP Id: rs1057517106

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132378377G>T , CM000667.2:g.132378377G>T GRCh38
NC_000005.9:g.131714069G>T , CM000667.1:g.131714069G>T GRCh37
NC_000005.8:g.131741968G>T NCBI36
NG_008982.1:g.13669G>T
NG_008982.2:g.13674G>T

Transcript Alleles

HGVS Amino-acid change
NM_001308122.1:c.466-1G>T VV NP_001295051.1:p.=
NM_003060.3:c.394-1G>T VV NP_003051.1:p.=
XR_427718.1:n.735-1G>T
XR_948290.1:n.735-1G>T
XR_948291.1:n.735-1G>T
XM_011543590.2:c.-238-1G>T XP_011541892.1:p.=
XM_017009778.2:c.-31-5770G>T XP_016865267.1:p.=
XR_001742215.1:n.735-1G>T
XR_001742216.1:n.735-1G>T
XR_427718.2:n.735-1G>T
XR_948290.2:n.735-1G>T
XR_948291.2:n.735-1G>T
ENST00000245407.7:c.394-1G>T ENSP00000245407.3:p.=
ENST00000415928.5:n.163-1G>T ENSP00000388838.1:p.=
ENST00000435065.6:n.466-1G>T ENSP00000402760.2:p.=
ENST00000437841.6:c.394-6951G>T ENSP00000400553.1:p.=
ENST00000461013.5:n.2151-1G>T