LDH info

Canonical Allele Identifier: CA15378974
Gene: XRCC4 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10040363

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.83177826A>G , CM000667.2:g.83177826A>G GRCh38
NC_000005.9:g.82473645A>G , CM000667.1:g.82473645A>G GRCh37
NC_000005.8:g.82509401A>G NCBI36
NG_047086.1:g.105418A>G

Transcript Alleles

HGVS Amino-acid change
NM_003401.3:c.316-17944A>G VV NP_003392.1:p.=
NM_022406.2:c.316-17944A>G VV NP_071801.1:p.=
NM_022550.2:c.316-17944A>G VV NP_072044.1:p.=
XM_005248595.1:c.316-17944A>G XP_005248652.1:p.=
XM_011543626.1:c.316-17944A>G XP_011541928.1:p.=
XM_011543627.1:c.316-17944A>G XP_011541929.1:p.=
XM_011543628.1:c.316-17944A>G XP_011541930.1:p.=
NM_001318012.1:c.316-17944A>G VV NP_001304941.1:p.=
NM_001318013.1:c.316-17944A>G VV NP_001304942.1:p.=
NM_003401.4:c.316-17944A>G VV NP_003392.1:p.=
NM_022406.3:c.316-17944A>G VV NP_071801.1:p.=
NM_022550.3:c.316-17944A>G VV NP_072044.1:p.=
XM_017009827.2:c.316-17944A>G XP_016865316.1:p.=
XM_017009828.2:c.316-17944A>G XP_016865317.1:p.=
XM_017009829.2:c.316-17944A>G XP_016865318.1:p.=
NM_001318012.2:c.316-17944A>G VV NP_001304941.1:p.=
NM_001318013.2:c.316-17944A>G VV NP_001304942.1:p.=
NM_003401.5:c.316-17944A>G VV MANE Preferred NP_003392.1:p.=
NM_022406.4:c.316-17944A>G VV NP_071801.1:p.=
ENST00000282268.7:c.316-17944A>G ENSP00000282268.3:p.=
ENST00000338635.10:c.316-17944A>G ENSP00000342011.6:p.=
ENST00000396027.8:c.316-17944A>G ENSP00000379344.4:p.=
ENST00000509268.1:n.328-17944A>G
ENST00000511817.1:c.316-17944A>G ENSP00000421491.1:p.=
ENST00000542685.5:n.385-17944A>G