Canonical Allele Identifier: CA913013104

Gene: RAD51C

Linked Data

• MyVariant Identifiers: chr17:g.56770014del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692654del , CM000679.2:g.58692654del	GRCh38
NC_000017.10:g.56770015del , CM000679.1:g.56770015del	GRCh37
NC_000017.9:g.54125014del	NCBI36
NG_023199.1:g.5053del , LRG_314:g.5053del
NG_047169.1:g.4427del

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.-238del	ENSP00000464056.2:n.-238del
ENST00000697675.1:n.82del
ENST00000697676.1:n.71del
ENST00000697677.1:n.69del
ENST00000697678.1:n.47+22del
ENST00000697679.1:n.62del
ENST00000697680.1:c.11del	ENSP00000513392.1:p.Lys4ArgfsTer12
ENST00000697681.1:c.11del	ENSP00000513393.1:p.Lys4ArgfsTer12
ENST00000697683.1:c.11del	ENSP00000513395.1:p.Lys4ArgfsTer12
ENST00000697684.1:n.71del
ENST00000697685.1:c.11del	ENSP00000513396.1:p.Lys4ArgfsTer12
ENST00000697686.1:c.-207+22del	ENSP00000513397.1:n.-207+22del
ENST00000697687.1:n.57del
ENST00000697688.1:n.57del
ENST00000697689.1:c.11del	ENSP00000513398.1:p.Lys4ArgfsTer12
ENST00000697690.1:c.11del	ENSP00000513399.1:p.Lys4ArgfsTer12
ENST00000697691.1:c.11del	ENSP00000513400.1:p.Lys4ArgfsTer11
ENST00000697692.1:c.11del	ENSP00000513401.1:p.Lys4ArgfsTer12
ENST00000337432.9:c.11del MANE Select	ENSP00000336701.4:p.Lys4ArgfsTer12
ENST00000337432.8:c.11del	ENSP00000336701.4:p.Lys4ArgfsTer12
ENST00000421782.3:c.11del	ENSP00000391450.2:p.Lys4ArgfsTer12
ENST00000461271.5:c.-238del	ENSP00000464056.1:n.-238del
ENST00000475762.5:c.11del	ENSP00000432421.1:p.Lys4ArgfsTer12
ENST00000476741.2:n.53del
ENST00000482007.5:c.11del	ENSP00000433332.1:p.Lys4ArgfsTer12
ENST00000486827.1:c.11del	ENSP00000436761.1:p.Lys4ArgfsTer12
ENST00000487525.5:c.11del	ENSP00000431637.1:p.Lys4ArgfsTer12
ENST00000487921.5:n.57+22del
ENST00000583539.5:c.11del	ENSP00000463121.1:p.Lys4ArgfsTer12
NM_002876.3:c.11del	NP_002867.1:p.Lys4ArgfsTer12
NM_058216.2:c.11del	NP_478123.1:p.Lys4ArgfsTer12
NR_103872.1:n.82del
NR_103873.1:n.82del
XM_006722001.2:c.11del	XP_006722064.1:p.Lys4ArgfsTer12
XM_006722002.2:c.11del	XP_006722065.1:p.Lys4ArgfsTer12
XM_006722004.2:c.-238del	XP_006722067.1:n.-238del
XM_006722005.2:c.-207+22del	XP_006722068.1:n.-207+22del
XM_011525092.1:c.-538del	XP_011523394.1:n.-538del
XM_011525093.1:c.-699del	XP_011523395.1:n.-699del
XR_934513.1:n.84del
XR_934514.1:n.84del
XM_006722001.4:c.11del	XP_006722064.1:p.Lys4ArgfsTer12
XM_006722002.4:c.11del	XP_006722065.1:p.Lys4ArgfsTer12
XM_006722004.3:c.-238del	XP_006722067.1:n.-238del
XM_006722005.3:c.-207+22del	XP_006722068.1:n.-207+22del
XM_017024914.1:c.-238del	XP_016880403.1:n.-238del
XM_017024916.1:c.-538del	XP_016880405.1:n.-538del
XM_017024917.1:c.-207+22del	XP_016880406.1:n.-207+22del
XM_017024918.2:c.-512del	XP_016880407.1:n.-512del
XR_934513.3:n.515del
XR_934514.3:n.515del
NM_058216.3:c.11del MANE Select	NP_478123.1:p.Lys4ArgfsTer12
NR_103872.2:n.53del
NM_002876.4:c.11del	NP_002867.1:p.Lys4ArgfsTer12