Canonical Allele Identifier: CA2809980353

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692606_58692614del , CM000679.2:g.58692606_58692614del	GRCh38
NC_000017.10:g.56769967_56769975del , CM000679.1:g.56769967_56769975del	GRCh37
NC_000017.9:g.54124966_54124974del	NCBI36
NG_023199.1:g.5005_5013del , LRG_314:g.5005_5013del
NG_047169.1:g.4466_4474del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-286_-278del	ENSP00000464056.2:n.-286_-278del
ENST00000697675.1:n.34_42del
ENST00000697676.1:n.23_31del
ENST00000697677.1:n.21_29del
ENST00000697678.1:n.21_29del
ENST00000697679.1:n.14_22del
ENST00000697680.1:c.-38_-30del	ENSP00000513392.1:n.-38_-30del
ENST00000697681.1:c.-38_-30del	ENSP00000513393.1:n.-38_-30del
ENST00000697683.1:c.-38_-30del	ENSP00000513395.1:n.-38_-30del
ENST00000697684.1:n.23_31del
ENST00000697685.1:c.-38_-30del	ENSP00000513396.1:n.-38_-30del
ENST00000697686.1:c.-233_-225del	ENSP00000513397.1:n.-233_-225del
ENST00000697687.1:n.9_17del
ENST00000697688.1:n.9_17del
ENST00000697689.1:c.-38_-30del	ENSP00000513398.1:n.-38_-30del
ENST00000697690.1:c.-38_-30del	ENSP00000513399.1:n.-38_-30del
ENST00000337432.9:c.-38_-30del MANE Select	ENSP00000336701.4:n.-38_-30del
ENST00000337432.8:c.-38_-30del	ENSP00000336701.4:n.-38_-30del
ENST00000461271.5:c.-286_-278del	ENSP00000464056.1:n.-286_-278del
ENST00000475762.5:c.-38_-30del	ENSP00000432421.1:n.-38_-30del
ENST00000476741.2:n.5_13del
ENST00000486827.1:c.-38_-30del	ENSP00000436761.1:n.-38_-30del
ENST00000487525.5:c.-38_-30del	ENSP00000431637.1:n.-38_-30del
ENST00000487921.5:n.31_39del
ENST00000583539.5:c.-38_-30del	ENSP00000463121.1:n.-38_-30del
NM_002876.3:c.-38_-30del	NP_002867.1:n.-38_-30del
NM_058216.2:c.-38_-30del	NP_478123.1:n.-38_-30del
NR_103872.1:n.34_42del
NR_103873.1:n.34_42del
XM_006722001.2:c.-38_-30del	XP_006722064.1:n.-38_-30del
XM_006722002.2:c.-38_-30del	XP_006722065.1:n.-38_-30del
XM_006722004.2:c.-286_-278del	XP_006722067.1:n.-286_-278del
XM_006722005.2:c.-233_-225del	XP_006722068.1:n.-233_-225del
XM_011525092.1:c.-586_-578del	XP_011523394.1:n.-586_-578del
XM_011525093.1:c.-747_-739del	XP_011523395.1:n.-747_-739del
XR_934513.1:n.36_44del
XR_934514.1:n.36_44del
XM_006722001.4:c.-38_-30del	XP_006722064.1:n.-38_-30del
XM_006722002.4:c.-38_-30del	XP_006722065.1:n.-38_-30del
XM_006722004.3:c.-286_-278del	XP_006722067.1:n.-286_-278del
XM_006722005.3:c.-233_-225del	XP_006722068.1:n.-233_-225del
XM_017024914.1:c.-286_-278del	XP_016880403.1:n.-286_-278del
XM_017024917.1:c.-233_-225del	XP_016880406.1:n.-233_-225del
XR_934513.3:n.467_475del
XR_934514.3:n.467_475del
NM_058216.3:c.-38_-30del MANE Select	NP_478123.1:n.-38_-30del
NR_103872.2:n.5_13del
NM_002876.4:c.-38_-30del	NP_002867.1:n.-38_-30del