LDH info

Canonical Allele Identifier: CA13291772
Gene: HK1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10159477

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69340132G>A , CM000672.2:g.69340132G>A GRCh38
NC_000010.10:g.71099888G>A , CM000672.1:g.71099888G>A GRCh37
NC_000010.9:g.70769894G>A NCBI36
NG_012077.1:g.75133G>A , LRG_365:g.75133G>A

Transcript Alleles

HGVS Amino-acid change
NM_000188.2:c.64-3695G>A VV NP_000179.2:p.=
NM_033496.2:c.61-3695G>A VV NP_277031.1:p.=
NM_033497.2:c.76-3695G>A VV NP_277032.1:p.=
NM_033498.2:c.76-3695G>A VV NP_277033.1:p.=
NM_033500.2:c.28-3695G>A , LRG_365t1:c.28-3695G>A NP_277035.2:p.=
XM_005269735.2:c.193-3695G>A XP_005269792.1:p.=
XM_005269736.1:c.76-3695G>A XP_005269793.1:p.=
XM_005269737.1:c.-22+1456G>A XP_005269794.1:p.=
XM_011539732.1:c.28-3695G>A XP_011538034.1:p.=
XM_011539733.1:c.22-3695G>A XP_011538035.1:p.=
XM_011539734.1:c.19-3695G>A XP_011538036.1:p.=
NM_001322364.1:c.76-3695G>A VV NP_001309293.1:p.=
NM_001322365.1:c.169-3695G>A VV NP_001309294.1:p.=
NM_001322366.1:c.-21-3695G>A VV NP_001309295.1:p.=
NM_001322367.1:c.64-3695G>A VV NP_001309296.1:p.=
NM_001358263.1:c.76-3695G>A VV NP_001345192.1:p.=
XM_024447969.1:c.76-3695G>A XP_024303737.1:p.=
ENST00000298649.7:c.61-3695G>A ENSP00000298649.3:p.=
ENST00000359426.6:c.64-3695G>A ENSP00000352398.6:p.=
ENST00000360289.6:c.28-3695G>A ENSP00000353433.2:p.=
ENST00000421088.5:c.28-3695G>A ENSP00000398316.1:p.=
ENST00000436817.5:c.61-3695G>A ENSP00000415949.1:p.=
ENST00000448642.6:c.76-3695G>A ENSP00000402103.3:p.=
ENST00000450646.5:c.76-3695G>A ENSP00000409761.1:p.=
ENST00000464803.5:n.434-3695G>A
ENST00000476368.5:n.443-3695G>A
ENST00000480047.5:n.558+1456G>A
ENST00000483054.5:n.529-3695G>A
ENST00000483077.5:n.468-3695G>A
ENST00000493591.5:n.68-3695G>A
ENST00000494253.1:n.289+1824G>A