Canonical Allele Identifier: CA2809980342

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692580_58692592del , CM000679.2:g.58692580_58692592del	GRCh38
NC_000017.10:g.56769941_56769953del , CM000679.1:g.56769941_56769953del	GRCh37
NC_000017.9:g.54124940_54124952del	NCBI36
NG_023199.1:g.4979_4991del , LRG_314:g.4979_4991del
NG_047169.1:g.4488_4500del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-312_-300del	ENSP00000464056.2:n.-312_-300del
ENST00000697675.1:n.8_20del
ENST00000697683.1:c.-64_-52del	ENSP00000513395.1:n.-64_-52del
ENST00000337432.8:c.-64_-52del	ENSP00000336701.4:n.-64_-52del
ENST00000461271.5:c.-312_-300del	ENSP00000464056.1:n.-312_-300del
ENST00000487921.5:n.5_17del
ENST00000583539.5:c.-64_-52del	ENSP00000463121.1:n.-64_-52del
NM_002876.3:c.-64_-52del	NP_002867.1:n.-64_-52del
NM_058216.2:c.-64_-52del	NP_478123.1:n.-64_-52del
NR_103872.1:n.8_20del
NR_103873.1:n.8_20del
XM_006722001.2:c.-64_-52del	XP_006722064.1:n.-64_-52del
XM_006722002.2:c.-64_-52del	XP_006722065.1:n.-64_-52del
XM_006722004.2:c.-312_-300del	XP_006722067.1:n.-312_-300del
XM_006722005.2:c.-259_-247del	XP_006722068.1:n.-259_-247del
XR_934513.1:n.10_22del
XR_934514.1:n.10_22del
XM_006722001.4:c.-64_-52del	XP_006722064.1:n.-64_-52del
XM_006722002.4:c.-64_-52del	XP_006722065.1:n.-64_-52del
XM_006722004.3:c.-312_-300del	XP_006722067.1:n.-312_-300del
XM_006722005.3:c.-259_-247del	XP_006722068.1:n.-259_-247del
XM_017024914.1:c.-312_-300del	XP_016880403.1:n.-312_-300del
XM_017024917.1:c.-259_-247del	XP_016880406.1:n.-259_-247del
XR_934513.3:n.441_453del
XR_934514.3:n.441_453del