LDH info

Canonical Allele Identifier: CA337454636
Gene: ZFY HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs13447361

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2953745G>C , CM000686.2:g.2953745G>C GRCh38
NC_000024.9:g.2821786G>C , CM000686.1:g.2821786G>C GRCh37
NC_000024.8:g.2881786G>C NCBI36
NG_008113.1:g.23241G>C

Transcript Alleles

HGVS Amino-acid change
NM_001145275.1:c.-17-7329G>C VV NP_001138747.1:p.=
NM_001145276.1:c.-28-164G>C VV NP_001138748.1:p.=
NM_003411.3:c.-28-164G>C VV NP_003402.2:p.=
XM_005262570.2:c.-28-164G>C XP_005262627.1:p.=
XM_006724873.2:c.-28-164G>C XP_006724936.1:p.=
XM_011531473.1:c.-17-7329G>C XP_011529775.1:p.=
XM_011531474.1:c.-17-7329G>C XP_011529776.1:p.=
XM_011531475.1:c.-28-164G>C XP_011529777.1:p.=
XM_011531473.2:c.-17-7329G>C XP_011529775.1:p.=
XM_011531474.2:c.-17-7329G>C XP_011529776.1:p.=
XM_011531475.3:c.-28-164G>C XP_011529777.1:p.=
XM_017030075.1:c.-28-164G>C XP_016885564.1:p.=
XM_017030076.1:c.-28-164G>C XP_016885565.1:p.=
XM_017030077.1:c.-17-7329G>C XP_016885566.1:p.=
NM_003411.4:c.-28-164G>C VV MANE Preferred NP_003402.2:p.=
ENST00000155093.7:c.-28-164G>C ENSP00000155093.3:p.=
ENST00000383052.5:c.-28-164G>C ENSP00000372525.1:p.=
ENST00000443793.1:c.-28-164G>C ENSP00000388814.1:p.=
ENST00000449237.4:c.-17-7329G>C ENSP00000393908.1:p.=
ENST00000469869.1:n.270+17976G>C
ENST00000625061.3:c.-28-164G>C ENSP00000485605.1:p.=