Canonical Allele Identifier: CA919868467

Gene: RAD51C

Linked Data

• dbSNP Id: rs1598511519

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58724148_58724149insATTTC , CM000679.2:g.58724148_58724149insATTTC	GRCh38
NC_000017.10:g.56801509_56801510insATTTC , CM000679.1:g.56801509_56801510insATTTC	GRCh37
NC_000017.9:g.54156508_54156509insATTTC	NCBI36
NG_023199.1:g.36547_36548insATTTC , LRG_314:g.36547_36548insATTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.614+48_614+49insATTTC	ENSP00000464056.2:n.614+48_614+49insATTTC
ENST00000697680.1:c.*1929+48_*1929+49insATTTC	ENSP00000513392.1:n.*1929+48_*1929+49insATTTC
ENST00000697681.1:c.*2126+48_*2126+49insATTTC	ENSP00000513393.1:n.*2126+48_*2126+49insATTTC
ENST00000697683.1:c.*1829+48_*1829+49insATTTC	ENSP00000513395.1:n.*1829+48_*1829+49insATTTC
ENST00000697684.1:n.1025+48_1025+49insATTTC
ENST00000697685.1:c.*1662+48_*1662+49insATTTC	ENSP00000513396.1:n.*1662+48_*1662+49insATTTC
ENST00000697686.1:c.614+48_614+49insATTTC	ENSP00000513397.1:n.614+48_614+49insATTTC
ENST00000697687.1:n.892_893insATTTC
ENST00000697688.1:n.1059_1060insATTTC
ENST00000697689.1:c.*1440+3336_*1440+3337insATTTC	ENSP00000513398.1:n.*1440+3336_*1440+3337insATTTC
ENST00000697690.1:c.904+3336_904+3337insATTTC	ENSP00000513399.1:n.904+3336_904+3337insATTTC
ENST00000697691.1:c.*937+48_*937+49insATTTC	ENSP00000513400.1:n.*937+48_*937+49insATTTC
ENST00000697692.1:c.*977+48_*977+49insATTTC	ENSP00000513401.1:n.*977+48_*977+49insATTTC
ENST00000697694.1:c.614+48_614+49insATTTC	ENSP00000513402.1:n.614+48_614+49insATTTC
ENST00000697695.1:n.1572+48_1572+49insATTTC
ENST00000337432.9:c.965+48_965+49insATTTC MANE Select	ENSP00000336701.4:n.965+48_965+49insATTTC
ENST00000337432.8:c.965+48_965+49insATTTC	ENSP00000336701.4:n.965+48_965+49insATTTC
ENST00000413590.5:c.603+48_603+49insATTTC
ENST00000475762.5:c.*1601+48_*1601+49insATTTC	ENSP00000432421.1:n.*1601+48_*1601+49insATTTC
ENST00000482007.5:c.*393+48_*393+49insATTTC	ENSP00000433332.1:n.*393+48_*393+49insATTTC
ENST00000487525.5:c.*538+48_*538+49insATTTC	ENSP00000431637.1:n.*538+48_*538+49insATTTC
ENST00000578151.1:n.239+3336_239+3337insATTTC
ENST00000581221.5:n.480+48_480+49insATTTC
ENST00000583539.5:c.965+48_965+49insATTTC	ENSP00000463121.1:n.965+48_965+49insATTTC
ENST00000584617.5:c.687+48_687+49insATTTC
ENST00000584804.1:c.199+3336_199+3337insATTTC	ENSP00000463658.1:n.199+3336_199+3337insATTTC
NM_058216.2:c.965+48_965+49insATTTC	NP_478123.1:n.965+48_965+49insATTTC
NR_103872.1:n.869+48_869+49insATTTC
XM_006722001.2:c.965+48_965+49insATTTC	XP_006722064.1:n.965+48_965+49insATTTC
XM_006722002.2:c.904+3336_904+3337insATTTC	XP_006722065.1:n.904+3336_904+3337insATTTC
XM_006722004.2:c.614+48_614+49insATTTC	XP_006722067.1:n.614+48_614+49insATTTC
XM_006722005.2:c.614+48_614+49insATTTC	XP_006722068.1:n.614+48_614+49insATTTC
XM_011525092.1:c.614+48_614+49insATTTC	XP_011523394.1:n.614+48_614+49insATTTC
XM_011525093.1:c.614+48_614+49insATTTC	XP_011523395.1:n.614+48_614+49insATTTC
XM_011525094.1:c.614+48_614+49insATTTC	XP_011523396.1:n.614+48_614+49insATTTC
XR_934513.1:n.1183+48_1183+49insATTTC
XR_934514.1:n.1183+48_1183+49insATTTC
XR_934886.1:n.427_428insAAATG
XM_006722001.4:c.965+48_965+49insATTTC	XP_006722064.1:n.965+48_965+49insATTTC
XM_006722002.4:c.904+3336_904+3337insATTTC	XP_006722065.1:n.904+3336_904+3337insATTTC
XM_006722004.3:c.614+48_614+49insATTTC	XP_006722067.1:n.614+48_614+49insATTTC
XM_006722005.3:c.614+48_614+49insATTTC	XP_006722068.1:n.614+48_614+49insATTTC
XM_011525092.2:c.614+48_614+49insATTTC	XP_011523394.1:n.614+48_614+49insATTTC
XM_011525093.2:c.614+48_614+49insATTTC	XP_011523395.1:n.614+48_614+49insATTTC
XM_011525094.2:c.614+48_614+49insATTTC	XP_011523396.1:n.614+48_614+49insATTTC
XM_017024914.1:c.614+48_614+49insATTTC	XP_016880403.1:n.614+48_614+49insATTTC
XM_017024915.1:c.614+48_614+49insATTTC	XP_016880404.1:n.614+48_614+49insATTTC
XM_017024916.1:c.614+48_614+49insATTTC	XP_016880405.1:n.614+48_614+49insATTTC
XM_017024917.1:c.614+48_614+49insATTTC	XP_016880406.1:n.614+48_614+49insATTTC
XM_017024918.2:c.614+48_614+49insATTTC	XP_016880407.1:n.614+48_614+49insATTTC
XM_017024919.1:c.553+3336_553+3337insATTTC	XP_016880408.1:n.553+3336_553+3337insATTTC
XR_934513.3:n.1614+48_1614+49insATTTC
XR_934514.3:n.1614+48_1614+49insATTTC
XR_934886.2:n.427_428insAAATG
NM_058216.3:c.965+48_965+49insATTTC MANE Select	NP_478123.1:n.965+48_965+49insATTTC
NR_103872.2:n.840+48_840+49insATTTC