LDH info

Canonical Allele Identifier: CA15590999
Gene: TMEM245 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1003346

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.109053060C>A , CM000671.2:g.109053060C>A GRCh38
NC_000009.11:g.111815340C>A , CM000671.1:g.111815340C>A GRCh37
NC_000009.10:g.110855161C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_032012.3:c.1855-2368G>T VV NP_114401.2:p.=
XM_011518446.1:c.1852-2368G>T XP_011516748.1:p.=
XM_011518447.1:c.1831-2368G>T XP_011516749.1:p.=
XM_011518448.1:c.1750-2368G>T XP_011516750.1:p.=
XM_011518449.1:c.1738-2368G>T XP_011516751.1:p.=
XM_011518450.1:c.1735-2368G>T XP_011516752.1:p.=
XM_011518451.1:c.1726-2368G>T XP_011516753.1:p.=
XM_011518452.1:c.1621-2368G>T XP_011516754.1:p.=
XR_930240.1:n.1392-21233C>A
XM_011518446.2:c.1852-2368G>T XP_011516748.1:p.=
XM_011518449.2:c.1738-2368G>T XP_011516751.1:p.=
XM_011518452.2:c.1621-2368G>T XP_011516754.1:p.=
XM_017014571.1:c.1828-2368G>T XP_016870060.1:p.=
XM_017014572.1:c.1597-2368G>T XP_016870061.1:p.=
NM_032012.4:c.1855-2368G>T VV MANE Preferred NP_114401.2:p.=
ENST00000374586.7:c.1855-2368G>T ENSP00000363714.3:p.=
ENST00000413712.6:n.632-2368G>T
ENST00000491854.1:c.*427-2368G>T ENSP00000417842.1:p.=