Canonical Allele Identifier: CA2267819452

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703218_58703225delinsTTTCACTC , CM000679.2:g.58703218_58703225delinsTTTCACTC	GRCh38
NC_000017.10:g.56780579_56780586delinsTTTCACTC , CM000679.1:g.56780579_56780586delinsTTTCACTC	GRCh37
NC_000017.9:g.54135578_54135585delinsTTTCACTC	NCBI36
NG_023199.1:g.15617_15624delinsTTTCACTC , LRG_314:g.15617_15624delinsTTTCACTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.243_250delinsTTTCACTC	ENSP00000464056.2:p.Asp81=
ENST00000697677.1:n.1675_1682delinsTTTCACTC
ENST00000697678.1:n.496_503delinsTTTCACTC
ENST00000697679.1:n.1668_1675delinsTTTCACTC
ENST00000697680.1:c.*1458_*1465delinsTTTCACTC	ENSP00000513392.1:n.*1458_*1465delinsTTTC...
ENST00000697681.1:c.*1610_*1617delinsTTTCACTC	ENSP00000513393.1:n.*1610_*1617delinsTTTC...
ENST00000697683.1:c.*1458_*1465delinsTTTCACTC	ENSP00000513395.1:n.*1458_*1465delinsTTTC...
ENST00000697684.1:n.654_661delinsTTTCACTC
ENST00000697685.1:c.*1291_*1298delinsTTTCACTC	ENSP00000513396.1:n.*1291_*1298delinsTTTC...
ENST00000697686.1:c.243_250delinsTTTCACTC	ENSP00000513397.1:p.Asp81=
ENST00000697687.1:n.473_480delinsTTTCACTC
ENST00000697688.1:n.640_647delinsTTTCACTC
ENST00000697689.1:c.*1130_*1137delinsTTTCACTC	ENSP00000513398.1:n.*1130_*1137delinsTTTC...
ENST00000697690.1:c.594_601delinsTTTCACTC	ENSP00000513399.1:p.Asp198=
ENST00000697691.1:c.*566_*573delinsTTTCACTC	ENSP00000513400.1:n.*566_*573delinsTTTCAC...
ENST00000697692.1:c.*606_*613delinsTTTCACTC	ENSP00000513401.1:n.*606_*613delinsTTTCAC...
ENST00000697694.1:c.243_250delinsTTTCACTC	ENSP00000513402.1:p.Asp81=
ENST00000697695.1:n.1201_1208delinsTTTCACTC
ENST00000337432.9:c.594_601delinsTTTCACTC MANE Select	ENSP00000336701.4:p.Asp198=
ENST00000337432.8:c.594_601delinsTTTCACTC	ENSP00000336701.4:p.Asp198=
ENST00000413590.5:c.232_239delinsTTTCACTC
ENST00000425173.5:c.390_397delinsTTTCACTC	ENSP00000407282.1:p.Asp130=
ENST00000461271.5:c.243_250delinsTTTCACTC	ENSP00000464056.1:p.Asp81=
ENST00000475762.5:c.*1297_*1304delinsTTTCACTC	ENSP00000432421.1:n.*1297_*1304delinsTTTC...
ENST00000482007.5:c.*22_*29delinsTTTCACTC	ENSP00000433332.1:n.*22_*29delinsTTTCACTC...
ENST00000487525.5:c.*22_*29delinsTTTCACTC	ENSP00000431637.1:n.*22_*29delinsTTTCACTC...
ENST00000487921.5:n.506_513delinsTTTCACTC
ENST00000583539.5:c.594_601delinsTTTCACTC	ENSP00000463121.1:p.Asp198=
ENST00000584617.5:c.316_323delinsTTTCACTC
NM_058216.2:c.594_601delinsTTTCACTC	NP_478123.1:p.Asp198=
NR_103872.1:n.498_505delinsTTTCACTC
XM_006722001.2:c.594_601delinsTTTCACTC	XP_006722064.1:p.Asp198=
XM_006722002.2:c.594_601delinsTTTCACTC	XP_006722065.1:p.Asp198=
XM_006722004.2:c.243_250delinsTTTCACTC	XP_006722067.1:p.Asp81=
XM_006722005.2:c.243_250delinsTTTCACTC	XP_006722068.1:p.Asp81=
XM_011525092.1:c.243_250delinsTTTCACTC	XP_011523394.1:p.Asp81=
XM_011525093.1:c.243_250delinsTTTCACTC	XP_011523395.1:p.Asp81=
XM_011525094.1:c.243_250delinsTTTCACTC	XP_011523396.1:p.Asp81=
XR_934513.1:n.667_674delinsTTTCACTC
XR_934514.1:n.667_674delinsTTTCACTC
XM_006722001.4:c.594_601delinsTTTCACTC	XP_006722064.1:p.Asp198=
XM_006722002.4:c.594_601delinsTTTCACTC	XP_006722065.1:p.Asp198=
XM_006722004.3:c.243_250delinsTTTCACTC	XP_006722067.1:p.Asp81=
XM_006722005.3:c.243_250delinsTTTCACTC	XP_006722068.1:p.Asp81=
XM_011525092.2:c.243_250delinsTTTCACTC	XP_011523394.1:p.Asp81=
XM_011525093.2:c.243_250delinsTTTCACTC	XP_011523395.1:p.Asp81=
XM_011525094.2:c.243_250delinsTTTCACTC	XP_011523396.1:p.Asp81=
XM_017024914.1:c.243_250delinsTTTCACTC	XP_016880403.1:p.Asp81=
XM_017024915.1:c.243_250delinsTTTCACTC	XP_016880404.1:p.Asp81=
XM_017024916.1:c.243_250delinsTTTCACTC	XP_016880405.1:p.Asp81=
XM_017024917.1:c.243_250delinsTTTCACTC	XP_016880406.1:p.Asp81=
XM_017024918.2:c.243_250delinsTTTCACTC	XP_016880407.1:p.Asp81=
XM_017024919.1:c.243_250delinsTTTCACTC	XP_016880408.1:p.Asp81=
XR_934513.3:n.1098_1105delinsTTTCACTC
XR_934514.3:n.1098_1105delinsTTTCACTC
NM_058216.3:c.594_601delinsTTTCACTC MANE Select	NP_478123.1:p.Asp198=
NR_103872.2:n.469_476delinsTTTCACTC