Canonical Allele Identifier: CA400341950

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58695173G>C , CM000679.2:g.58695173G>C	GRCh38
NC_000017.10:g.56772534G>C , CM000679.1:g.56772534G>C	GRCh37
NC_000017.9:g.54127533G>C	NCBI36
NG_023199.1:g.7572G>C , LRG_314:g.7572G>C
NG_047169.1:g.1907C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_058216.3:c.388G>C MANE Select	NP_478123.1:p.Gly130Arg
ENST00000337432.9:c.388G>C MANE Select	ENSP00000336701.4:p.Gly130Arg
NM_002876.3:c.388G>C	NP_002867.1:p.Gly130Arg
NM_002876.4:c.388G>C	NP_002867.1:p.Gly130Arg
NM_058216.2:c.388G>C	NP_478123.1:p.Gly130Arg
NR_103872.1:n.459G>C
NR_103872.2:n.430G>C
NR_103873.1:n.356G>C
ENST00000337432.8:c.388G>C	ENSP00000336701.4:p.Gly130Arg
ENST00000413590.5:c.26G>C
ENST00000421782.3:c.388G>C	ENSP00000391450.2:p.Gly130Arg
ENST00000425173.5:c.184G>C	ENSP00000407282.1:p.Gly62Arg
ENST00000461271.5:c.37G>C	ENSP00000464056.1:p.Gly13Arg
ENST00000461271.6:c.37G>C	ENSP00000464056.2:p.Gly13Arg
ENST00000475762.5:c.*1091G>C	ENSP00000432421.1:n.*1091G>C
ENST00000482007.5:c.388G>C	ENSP00000433332.1:p.Gly130Arg
ENST00000486827.1:c.*1252G>C	ENSP00000436761.1:n.*1252G>C
ENST00000487525.5:c.388G>C	ENSP00000431637.1:p.Gly130Arg
ENST00000487921.5:n.300G>C
ENST00000583539.5:c.388G>C	ENSP00000463121.1:p.Gly130Arg
ENST00000584617.5:c.127-1520G>C
ENST00000622327.4:c.124G>C	ENSP00000482326.1:p.Gly42Arg
ENST00000697675.1:n.1482G>C
ENST00000697676.1:n.448G>C
ENST00000697677.1:n.1469G>C
ENST00000697678.1:n.290G>C
ENST00000697679.1:n.1462G>C
ENST00000697680.1:c.*1252G>C	ENSP00000513392.1:n.*1252G>C
ENST00000697681.1:c.*1252G>C	ENSP00000513393.1:n.*1252G>C
ENST00000697683.1:c.*1252G>C	ENSP00000513395.1:n.*1252G>C
ENST00000697684.1:n.448G>C
ENST00000697685.1:c.*1252G>C	ENSP00000513396.1:n.*1252G>C
ENST00000697686.1:c.37G>C	ENSP00000513397.1:p.Gly13Arg
ENST00000697687.1:n.434G>C
ENST00000697688.1:n.434G>C
ENST00000697689.1:c.*1091G>C	ENSP00000513398.1:n.*1091G>C
ENST00000697690.1:c.388G>C	ENSP00000513399.1:p.Gly130Arg
ENST00000697691.1:c.*360G>C	ENSP00000513400.1:n.*360G>C
ENST00000697692.1:c.*400G>C	ENSP00000513401.1:n.*400G>C
ENST00000697693.1:n.1163G>C
ENST00000697694.1:c.37G>C	ENSP00000513402.1:p.Gly13Arg
ENST00000697695.1:n.995G>C
XM_006722001.2:c.388G>C	XP_006722064.1:p.Gly130Arg
XM_006722001.4:c.388G>C	XP_006722064.1:p.Gly130Arg
XM_006722002.2:c.388G>C	XP_006722065.1:p.Gly130Arg
XM_006722002.4:c.388G>C	XP_006722065.1:p.Gly130Arg
XM_006722004.2:c.37G>C	XP_006722067.1:p.Gly13Arg
XM_006722004.3:c.37G>C	XP_006722067.1:p.Gly13Arg
XM_006722005.2:c.37G>C	XP_006722068.1:p.Gly13Arg
XM_006722005.3:c.37G>C	XP_006722068.1:p.Gly13Arg
XM_011525092.1:c.37G>C	XP_011523394.1:p.Gly13Arg
XM_011525092.2:c.37G>C	XP_011523394.1:p.Gly13Arg
XM_011525093.1:c.37G>C	XP_011523395.1:p.Gly13Arg
XM_011525093.2:c.37G>C	XP_011523395.1:p.Gly13Arg
XM_011525094.1:c.37G>C	XP_011523396.1:p.Gly13Arg
XM_011525094.2:c.37G>C	XP_011523396.1:p.Gly13Arg
XM_017024914.1:c.37G>C	XP_016880403.1:p.Gly13Arg
XM_017024915.1:c.37G>C	XP_016880404.1:p.Gly13Arg
XM_017024916.1:c.37G>C	XP_016880405.1:p.Gly13Arg
XM_017024917.1:c.37G>C	XP_016880406.1:p.Gly13Arg
XM_017024918.2:c.37G>C	XP_016880407.1:p.Gly13Arg
XM_017024919.1:c.37G>C	XP_016880408.1:p.Gly13Arg
XR_934513.1:n.461G>C
XR_934513.3:n.892G>C
XR_934514.1:n.461G>C
XR_934514.3:n.892G>C