Canonical Allele Identifier: CA2267829078

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58724037_58724038delinsCA , CM000679.2:g.58724037_58724038delinsCA	GRCh38
NC_000017.10:g.56801398_56801399delinsCA , CM000679.1:g.56801398_56801399delinsCA	GRCh37
NC_000017.9:g.54156397_54156398delinsCA	NCBI36
NG_023199.1:g.36436_36437delinsCA , LRG_314:g.36436_36437delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.554-3_554-2delinsCA	ENSP00000464056.2:n.554-3_554-2delinsCA
ENST00000697680.1:c.*1869-3_*1869-2delinsCA	ENSP00000513392.1:n.*1869-3_*1869-2delinsCA
ENST00000697681.1:c.*2066-3_*2066-2delinsCA	ENSP00000513393.1:n.*2066-3_*2066-2delinsCA
ENST00000697683.1:c.*1769-3_*1769-2delinsCA	ENSP00000513395.1:n.*1769-3_*1769-2delinsCA
ENST00000697684.1:n.965-3_965-2delinsCA
ENST00000697685.1:c.*1602-3_*1602-2delinsCA	ENSP00000513396.1:n.*1602-3_*1602-2delinsCA
ENST00000697686.1:c.554-3_554-2delinsCA	ENSP00000513397.1:n.554-3_554-2delinsCA
ENST00000697687.1:n.784-3_784-2delinsCA
ENST00000697688.1:n.951-3_951-2delinsCA
ENST00000697689.1:c.*1440+3225_*1440+3226delinsCA	ENSP00000513398.1:n.*1440+3225_*1440+3226delinsCA
ENST00000697690.1:c.904+3225_904+3226delinsCA	ENSP00000513399.1:n.904+3225_904+3226delinsCA
ENST00000697691.1:c.*877-3_*877-2delinsCA	ENSP00000513400.1:n.*877-3_*877-2delinsCA
ENST00000697692.1:c.*917-3_*917-2delinsCA	ENSP00000513401.1:n.*917-3_*917-2delinsCA
ENST00000697694.1:c.554-3_554-2delinsCA	ENSP00000513402.1:n.554-3_554-2delinsCA
ENST00000697695.1:n.1512-3_1512-2delinsCA
ENST00000337432.9:c.905-3_905-2delinsCA MANE Select	ENSP00000336701.4:n.905-3_905-2delinsCA
ENST00000337432.8:c.905-3_905-2delinsCA	ENSP00000336701.4:n.905-3_905-2delinsCA
ENST00000413590.5:c.543-3_543-2delinsCA
ENST00000475762.5:c.*1541-3_*1541-2delinsCA	ENSP00000432421.1:n.*1541-3_*1541-2delinsCA
ENST00000482007.5:c.*333-3_*333-2delinsCA	ENSP00000433332.1:n.*333-3_*333-2delinsCA
ENST00000487525.5:c.*478-3_*478-2delinsCA	ENSP00000431637.1:n.*478-3_*478-2delinsCA
ENST00000578151.1:n.239+3225_239+3226delinsCA
ENST00000581221.5:n.420-3_420-2delinsCA
ENST00000583539.5:c.905-3_905-2delinsCA	ENSP00000463121.1:n.905-3_905-2delinsCA
ENST00000584617.5:c.627-3_627-2delinsCA
ENST00000584804.1:c.199+3225_199+3226delinsCA	ENSP00000463658.1:n.199+3225_199+3226delinsCA
NM_058216.2:c.905-3_905-2delinsCA	NP_478123.1:n.905-3_905-2delinsCA
NR_103872.1:n.809-3_809-2delinsCA
XM_006722001.2:c.905-3_905-2delinsCA	XP_006722064.1:n.905-3_905-2delinsCA
XM_006722002.2:c.904+3225_904+3226delinsCA	XP_006722065.1:n.904+3225_904+3226delinsCA
XM_006722004.2:c.554-3_554-2delinsCA	XP_006722067.1:n.554-3_554-2delinsCA
XM_006722005.2:c.554-3_554-2delinsCA	XP_006722068.1:n.554-3_554-2delinsCA
XM_011525092.1:c.554-3_554-2delinsCA	XP_011523394.1:n.554-3_554-2delinsCA
XM_011525093.1:c.554-3_554-2delinsCA	XP_011523395.1:n.554-3_554-2delinsCA
XM_011525094.1:c.554-3_554-2delinsCA	XP_011523396.1:n.554-3_554-2delinsCA
XR_934513.1:n.1123-3_1123-2delinsCA
XR_934514.1:n.1123-3_1123-2delinsCA
XM_006722001.4:c.905-3_905-2delinsCA	XP_006722064.1:n.905-3_905-2delinsCA
XM_006722002.4:c.904+3225_904+3226delinsCA	XP_006722065.1:n.904+3225_904+3226delinsCA
XM_006722004.3:c.554-3_554-2delinsCA	XP_006722067.1:n.554-3_554-2delinsCA
XM_006722005.3:c.554-3_554-2delinsCA	XP_006722068.1:n.554-3_554-2delinsCA
XM_011525092.2:c.554-3_554-2delinsCA	XP_011523394.1:n.554-3_554-2delinsCA
XM_011525093.2:c.554-3_554-2delinsCA	XP_011523395.1:n.554-3_554-2delinsCA
XM_011525094.2:c.554-3_554-2delinsCA	XP_011523396.1:n.554-3_554-2delinsCA
XM_017024914.1:c.554-3_554-2delinsCA	XP_016880403.1:n.554-3_554-2delinsCA
XM_017024915.1:c.554-3_554-2delinsCA	XP_016880404.1:n.554-3_554-2delinsCA
XM_017024916.1:c.554-3_554-2delinsCA	XP_016880405.1:n.554-3_554-2delinsCA
XM_017024917.1:c.554-3_554-2delinsCA	XP_016880406.1:n.554-3_554-2delinsCA
XM_017024918.2:c.554-3_554-2delinsCA	XP_016880407.1:n.554-3_554-2delinsCA
XM_017024919.1:c.553+3225_553+3226delinsCA	XP_016880408.1:n.553+3225_553+3226delinsCA
XR_934513.3:n.1554-3_1554-2delinsCA
XR_934514.3:n.1554-3_1554-2delinsCA
NM_058216.3:c.905-3_905-2delinsCA MANE Select	NP_478123.1:n.905-3_905-2delinsCA
NR_103872.2:n.780-3_780-2delinsCA