LDH info

Canonical Allele Identifier: CA8677143
Gene: RAD51C HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs760830928

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692723_58692742del , CM000679.2:g.58692723_58692742del GRCh38
NC_000017.10:g.56770084_56770103del , CM000679.1:g.56770084_56770103del GRCh37
NC_000017.9:g.54125083_54125102del NCBI36
NG_023199.1:g.5122_5141del , LRG_314:g.5122_5141del
NG_047169.1:g.4338_4357del

Transcript Alleles

HGVS Amino-acid change
NM_002876.3:c.80_99del VV NP_002867.1:p.Leu27HisfsTer3
NM_058216.2:c.80_99del VV NP_478123.1:p.Leu27HisfsTer3
NR_103872.1:n.151_170del
NR_103873.1:n.113+38_113+57del
XM_006722001.2:c.80_99del XP_006722064.1:p.Leu27HisfsTer3
XM_006722002.2:c.80_99del XP_006722065.1:p.Leu27HisfsTer3
XM_006722004.2:c.-207+38_-207+57del XP_006722067.1:p.=
XM_006722005.2:c.-207+91_-207+110del XP_006722068.1:p.=
XM_011525092.1:c.-507+38_-507+57del XP_011523394.1:p.=
XM_011525093.1:c.-668+38_-668+57del XP_011523395.1:p.=
XR_934513.1:n.153_172del
XR_934514.1:n.153_172del
XM_006722001.4:c.80_99del XP_006722064.1:p.Leu27HisfsTer3
XM_006722002.4:c.80_99del XP_006722065.1:p.Leu27HisfsTer3
XM_006722004.3:c.-207+38_-207+57del XP_006722067.1:p.=
XM_006722005.3:c.-207+91_-207+110del XP_006722068.1:p.=
XM_011525092.2:c.-507+38_-507+57del XP_011523394.1:p.=
XM_011525093.2:c.-668+38_-668+57del XP_011523395.1:p.=
XM_017024914.1:c.-207+38_-207+57del XP_016880403.1:p.=
XM_017024916.1:c.-507+38_-507+57del XP_016880405.1:p.=
XM_017024917.1:c.-207+91_-207+110del XP_016880406.1:p.=
XM_017024918.2:c.-443_-424del XP_016880407.1:p.=
XM_017024919.1:c.-668+38_-668+57del XP_016880408.1:p.=
XR_934513.3:n.584_603del
XR_934514.3:n.584_603del
NM_058216.3:c.80_99del VV MANE Preferred NP_478123.1:p.Leu27HisfsTer3
ENST00000337432.8:c.80_99del ENSP00000336701.4:p.Leu27HisfsTer3
ENST00000421782.3:c.80_99del ENSP00000391450.2:p.Leu27HisfsTer3
ENST00000461271.5:c.-207+38_-207+57del ENSP00000464056.1:p.=
ENST00000475762.5:c.80_99del ENSP00000432421.1:p.Leu27HisfsTer3
ENST00000476741.2:n.122_141del
ENST00000482007.5:c.80_99del ENSP00000433332.1:p.Leu27HisfsTer3
ENST00000486827.1:c.80_99del ENSP00000436761.1:p.Leu27HisfsTer3
ENST00000487525.5:c.80_99del ENSP00000431637.1:p.Leu27HisfsTer3
ENST00000487921.5:n.57+91_57+110del
ENST00000583539.5:c.80_99del ENSP00000463121.1:p.Leu27HisfsTer3
ENST00000584617.5:n.61_80del