LDH info

Canonical Allele Identifier: CA12787294
Gene: CLU HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11136000

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27607002T>C , CM000670.2:g.27607002T>C GRCh38
NC_000008.10:g.27464519T>C , CM000670.1:g.27464519T>C GRCh37
NC_000008.9:g.27520436T>C NCBI36
NG_027845.1:g.12809A>G

Transcript Alleles

HGVS Amino-acid change
NM_001831.3:c.247-478A>G VV NP_001822.3:p.=
NR_038335.1:n.568-478A>G
NR_045494.1:n.427-478A>G
XM_006716284.1:c.403-478A>G XP_006716347.1:p.=
XM_006716284.3:c.403-478A>G XP_006716347.1:p.=
NM_001831.4:c.247-478A>G VV MANE Preferred NP_001822.3:p.=
ENST00000316403.14:c.247-478A>G ENSP00000315130.10:p.=
ENST00000405140.7:c.247-478A>G ENSP00000385419.3:p.=
ENST00000519742.5:c.247-478A>G ENSP00000431026.1:p.=
ENST00000520491.5:c.247-478A>G ENSP00000429881.1:p.=
ENST00000520796.5:c.247-478A>G ENSP00000429336.1:p.=
ENST00000522299.5:n.315-478A>G
ENST00000522413.5:c.247-478A>G ENSP00000428779.1:p.=
ENST00000523500.5:c.247-478A>G ENSP00000429620.1:p.=
ENST00000523589.5:c.247-478A>G ENSP00000431070.1:p.=
ENST00000560566.5:c.280-478A>G ENSP00000453247.1:p.=