Canonical Allele Identifier: CA400354128

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709952C>T , CM000679.2:g.58709952C>T	GRCh38
NC_000017.10:g.56787313C>T , CM000679.1:g.56787313C>T	GRCh37
NC_000017.9:g.54142312C>T	NCBI36
NG_023199.1:g.22351C>T , LRG_314:g.22351C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_058216.3:c.799C>T MANE Select	NP_478123.1:p.Gln267Ter
ENST00000337432.9:c.799C>T MANE Select	ENSP00000336701.4:p.Gln267Ter
NM_058216.2:c.799C>T	NP_478123.1:p.Gln267Ter
NR_103872.1:n.703C>T
NR_103872.2:n.674C>T
ENST00000337432.8:c.799C>T	ENSP00000336701.4:p.Gln267Ter
ENST00000413590.5:c.437C>T
ENST00000461271.6:c.448C>T	ENSP00000464056.2:p.Gln150Ter
ENST00000475762.5:c.*1502C>T	ENSP00000432421.1:n.*1502C>T
ENST00000482007.5:c.*227C>T	ENSP00000433332.1:n.*227C>T
ENST00000487525.5:c.*372C>T	ENSP00000431637.1:n.*372C>T
ENST00000578151.1:n.134C>T
ENST00000581221.5:n.314C>T
ENST00000583539.5:c.799C>T	ENSP00000463121.1:p.Gln267Ter
ENST00000584617.5:c.521C>T
ENST00000584804.1:c.94C>T	ENSP00000463658.1:p.Gln32Ter
ENST00000697678.1:n.701C>T
ENST00000697679.1:n.1873C>T
ENST00000697680.1:c.*1663C>T	ENSP00000513392.1:n.*1663C>T
ENST00000697681.1:c.*1960C>T	ENSP00000513393.1:n.*1960C>T
ENST00000697683.1:c.*1663C>T	ENSP00000513395.1:n.*1663C>T
ENST00000697684.1:n.859C>T
ENST00000697685.1:c.*1496C>T	ENSP00000513396.1:n.*1496C>T
ENST00000697686.1:c.448C>T	ENSP00000513397.1:p.Gln150Ter
ENST00000697687.1:n.678C>T
ENST00000697688.1:n.845C>T
ENST00000697689.1:c.*1335C>T	ENSP00000513398.1:n.*1335C>T
ENST00000697690.1:c.799C>T	ENSP00000513399.1:p.Gln267Ter
ENST00000697691.1:c.*771C>T	ENSP00000513400.1:n.*771C>T
ENST00000697692.1:c.*811C>T	ENSP00000513401.1:n.*811C>T
ENST00000697694.1:c.448C>T	ENSP00000513402.1:p.Gln150Ter
ENST00000697695.1:n.1406C>T
XM_006722001.2:c.799C>T	XP_006722064.1:p.Gln267Ter
XM_006722001.4:c.799C>T	XP_006722064.1:p.Gln267Ter
XM_006722002.2:c.799C>T	XP_006722065.1:p.Gln267Ter
XM_006722002.4:c.799C>T	XP_006722065.1:p.Gln267Ter
XM_006722004.2:c.448C>T	XP_006722067.1:p.Gln150Ter
XM_006722004.3:c.448C>T	XP_006722067.1:p.Gln150Ter
XM_006722005.2:c.448C>T	XP_006722068.1:p.Gln150Ter
XM_006722005.3:c.448C>T	XP_006722068.1:p.Gln150Ter
XM_011525092.1:c.448C>T	XP_011523394.1:p.Gln150Ter
XM_011525092.2:c.448C>T	XP_011523394.1:p.Gln150Ter
XM_011525093.1:c.448C>T	XP_011523395.1:p.Gln150Ter
XM_011525093.2:c.448C>T	XP_011523395.1:p.Gln150Ter
XM_011525094.1:c.448C>T	XP_011523396.1:p.Gln150Ter
XM_011525094.2:c.448C>T	XP_011523396.1:p.Gln150Ter
XM_017024914.1:c.448C>T	XP_016880403.1:p.Gln150Ter
XM_017024915.1:c.448C>T	XP_016880404.1:p.Gln150Ter
XM_017024916.1:c.448C>T	XP_016880405.1:p.Gln150Ter
XM_017024917.1:c.448C>T	XP_016880406.1:p.Gln150Ter
XM_017024918.2:c.448C>T	XP_016880407.1:p.Gln150Ter
XM_017024919.1:c.448C>T	XP_016880408.1:p.Gln150Ter
XR_934513.1:n.1017C>T
XR_934513.3:n.1448C>T
XR_934514.1:n.1017C>T
XR_934514.3:n.1448C>T