Canonical Allele Identifier: CA400341876

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58695162C>T , CM000679.2:g.58695162C>T	GRCh38
NC_000017.10:g.56772523C>T , CM000679.1:g.56772523C>T	GRCh37
NC_000017.9:g.54127522C>T	NCBI36
NG_023199.1:g.7561C>T , LRG_314:g.7561C>T
NG_047169.1:g.1918G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_058216.3:c.377C>T MANE Select	NP_478123.1:p.Ala126Val
ENST00000337432.9:c.377C>T MANE Select	ENSP00000336701.4:p.Ala126Val
NM_002876.3:c.377C>T	NP_002867.1:p.Ala126Val
NM_002876.4:c.377C>T	NP_002867.1:p.Ala126Val
NM_058216.2:c.377C>T	NP_478123.1:p.Ala126Val
NR_103872.1:n.448C>T
NR_103872.2:n.419C>T
NR_103873.1:n.345C>T
ENST00000337432.8:c.377C>T	ENSP00000336701.4:p.Ala126Val
ENST00000413590.5:c.15C>T
ENST00000421782.3:c.377C>T	ENSP00000391450.2:p.Ala126Val
ENST00000425173.5:c.173C>T	ENSP00000407282.1:p.Ala58Val
ENST00000461271.5:c.26C>T	ENSP00000464056.1:p.Ala9Val
ENST00000461271.6:c.26C>T	ENSP00000464056.2:p.Ala9Val
ENST00000475762.5:c.*1080C>T	ENSP00000432421.1:n.*1080C>T
ENST00000482007.5:c.377C>T	ENSP00000433332.1:p.Ala126Val
ENST00000486827.1:c.*1241C>T	ENSP00000436761.1:n.*1241C>T
ENST00000487525.5:c.377C>T	ENSP00000431637.1:p.Ala126Val
ENST00000487921.5:n.289C>T
ENST00000583539.5:c.377C>T	ENSP00000463121.1:p.Ala126Val
ENST00000584617.5:c.127-1531C>T
ENST00000622327.4:c.113C>T	ENSP00000482326.1:p.Ala38Val
ENST00000697675.1:n.1471C>T
ENST00000697676.1:n.437C>T
ENST00000697677.1:n.1458C>T
ENST00000697678.1:n.279C>T
ENST00000697679.1:n.1451C>T
ENST00000697680.1:c.*1241C>T	ENSP00000513392.1:n.*1241C>T
ENST00000697681.1:c.*1241C>T	ENSP00000513393.1:n.*1241C>T
ENST00000697683.1:c.*1241C>T	ENSP00000513395.1:n.*1241C>T
ENST00000697684.1:n.437C>T
ENST00000697685.1:c.*1241C>T	ENSP00000513396.1:n.*1241C>T
ENST00000697686.1:c.26C>T	ENSP00000513397.1:p.Ala9Val
ENST00000697687.1:n.423C>T
ENST00000697688.1:n.423C>T
ENST00000697689.1:c.*1080C>T	ENSP00000513398.1:n.*1080C>T
ENST00000697690.1:c.377C>T	ENSP00000513399.1:p.Ala126Val
ENST00000697691.1:c.*349C>T	ENSP00000513400.1:n.*349C>T
ENST00000697692.1:c.*389C>T	ENSP00000513401.1:n.*389C>T
ENST00000697693.1:n.1152C>T
ENST00000697694.1:c.26C>T	ENSP00000513402.1:p.Ala9Val
ENST00000697695.1:n.984C>T
XM_006722001.2:c.377C>T	XP_006722064.1:p.Ala126Val
XM_006722001.4:c.377C>T	XP_006722064.1:p.Ala126Val
XM_006722002.2:c.377C>T	XP_006722065.1:p.Ala126Val
XM_006722002.4:c.377C>T	XP_006722065.1:p.Ala126Val
XM_006722004.2:c.26C>T	XP_006722067.1:p.Ala9Val
XM_006722004.3:c.26C>T	XP_006722067.1:p.Ala9Val
XM_006722005.2:c.26C>T	XP_006722068.1:p.Ala9Val
XM_006722005.3:c.26C>T	XP_006722068.1:p.Ala9Val
XM_011525092.1:c.26C>T	XP_011523394.1:p.Ala9Val
XM_011525092.2:c.26C>T	XP_011523394.1:p.Ala9Val
XM_011525093.1:c.26C>T	XP_011523395.1:p.Ala9Val
XM_011525093.2:c.26C>T	XP_011523395.1:p.Ala9Val
XM_011525094.1:c.26C>T	XP_011523396.1:p.Ala9Val
XM_011525094.2:c.26C>T	XP_011523396.1:p.Ala9Val
XM_017024914.1:c.26C>T	XP_016880403.1:p.Ala9Val
XM_017024915.1:c.26C>T	XP_016880404.1:p.Ala9Val
XM_017024916.1:c.26C>T	XP_016880405.1:p.Ala9Val
XM_017024917.1:c.26C>T	XP_016880406.1:p.Ala9Val
XM_017024918.2:c.26C>T	XP_016880407.1:p.Ala9Val
XM_017024919.1:c.26C>T	XP_016880408.1:p.Ala9Val
XR_934513.1:n.450C>T
XR_934513.3:n.881C>T
XR_934514.1:n.450C>T
XR_934514.3:n.881C>T