LDH info

Canonical Allele Identifier: CA12014457
Gene: RNF145 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10076782

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159177955G>A , CM000667.2:g.159177955G>A GRCh38
NC_000005.9:g.158604963G>A , CM000667.1:g.158604963G>A GRCh37
NC_000005.8:g.158537541G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001199380.1:c.476-1088C>T VV NP_001186309.1:p.=
NM_001199381.1:c.437-1088C>T VV NP_001186310.1:p.=
NM_001199382.1:c.428-1088C>T VV NP_001186311.1:p.=
NM_001199383.1:c.386-1088C>T VV NP_001186312.1:p.=
NM_144726.2:c.470-1088C>T VV NP_653327.1:p.=
XM_005265826.3:c.434-1088C>T XP_005265883.1:p.=
XM_017009138.2:c.386-1088C>T XP_016864627.1:p.=
XM_024454383.1:c.434-1088C>T XP_024310151.1:p.=
NM_001199381.2:c.437-1088C>T VV NP_001186310.1:p.=
NM_001199383.2:c.386-1088C>T VV NP_001186312.1:p.=
ENST00000274542.6:c.470-1088C>T ENSP00000274542.2:p.=
ENST00000424310.6:c.386-1088C>T ENSP00000409064.2:p.=
ENST00000518802.5:c.476-1088C>T ENSP00000430955.1:p.=
ENST00000519865.5:c.386-1088C>T ENSP00000430397.1:p.=
ENST00000520638.1:c.428-1088C>T ENSP00000429071.1:p.=
ENST00000521606.6:c.437-1088C>T ENSP00000430753.2:p.=
ENST00000611185.4:c.386-1088C>T ENSP00000482720.1:p.=