Canonical Allele Identifier: CA2638988617
Gene: RAD51C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692578_58692580del , CM000679.2:g.58692578_58692580del GRCh38
NC_000017.10:g.56769939_56769941del , CM000679.1:g.56769939_56769941del GRCh37
NC_000017.9:g.54124938_54124940del NCBI36
NG_023199.1:g.4977_4979del , LRG_314:g.4977_4979del
NG_047169.1:g.4500_4502del

Transcript Alleles

HGVS Amino-acid change
ENST00000461271.6:c.-314_-312del ENSP00000464056.2:n.-314_-312del
ENST00000697675.1:n.6_8del
ENST00000337432.8:c.-66_-64del ENSP00000336701.4:n.-66_-64del
ENST00000461271.5:c.-314_-312del ENSP00000464056.1:n.-314_-312del
ENST00000487921.5:n.3_5del
ENST00000583539.5:c.-66_-64del ENSP00000463121.1:n.-66_-64del
NM_002876.3:c.-66_-64del NP_002867.1:n.-66_-64del
NM_058216.2:c.-66_-64del NP_478123.1:n.-66_-64del
NR_103872.1:n.6_8del
NR_103873.1:n.6_8del
XM_006722001.2:c.-66_-64del XP_006722064.1:n.-66_-64del
XM_006722002.2:c.-66_-64del XP_006722065.1:n.-66_-64del
XM_006722004.2:c.-314_-312del XP_006722067.1:n.-314_-312del
XM_006722005.2:c.-261_-259del XP_006722068.1:n.-261_-259del
XR_934513.1:n.8_10del
XR_934514.1:n.8_10del
XM_006722001.4:c.-66_-64del XP_006722064.1:n.-66_-64del
XM_006722002.4:c.-66_-64del XP_006722065.1:n.-66_-64del
XM_006722004.3:c.-314_-312del XP_006722067.1:n.-314_-312del
XM_006722005.3:c.-261_-259del XP_006722068.1:n.-261_-259del
XM_017024914.1:c.-314_-312del XP_016880403.1:n.-314_-312del
XM_017024917.1:c.-261_-259del XP_016880406.1:n.-261_-259del
XR_934513.3:n.439_441del
XR_934514.3:n.439_441del