Canonical Allele Identifier: CA8677347

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58720791G>A , CM000679.2:g.58720791G>A	GRCh38
NC_000017.10:g.56798152G>A , CM000679.1:g.56798152G>A	GRCh37
NC_000017.9:g.54153151G>A	NCBI36
NG_023199.1:g.33190G>A , LRG_314:g.33190G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_058216.3:c.883G>A MANE Select	NP_478123.1:p.Ala295Thr
ENST00000337432.9:c.883G>A MANE Select	ENSP00000336701.4:p.Ala295Thr
NM_058216.2:c.883G>A	NP_478123.1:p.Ala295Thr
NR_103872.1:n.787G>A
NR_103872.2:n.758G>A
ENST00000337432.8:c.883G>A	ENSP00000336701.4:p.Ala295Thr
ENST00000413590.5:c.521G>A
ENST00000461271.6:c.532G>A	ENSP00000464056.2:p.Ala178Thr
ENST00000475762.5:c.*1541-3249G>A	ENSP00000432421.1:n.*1541-3249G>A
ENST00000482007.5:c.*311G>A	ENSP00000433332.1:n.*311G>A
ENST00000487525.5:c.*456G>A	ENSP00000431637.1:n.*456G>A
ENST00000578151.1:n.218G>A
ENST00000581221.5:n.398G>A
ENST00000583539.5:c.883G>A	ENSP00000463121.1:p.Ala295Thr
ENST00000584617.5:c.605G>A
ENST00000584804.1:c.178G>A	ENSP00000463658.1:p.Ala60Thr
ENST00000697678.1:n.785G>A
ENST00000697679.1:n.1957G>A
ENST00000697680.1:c.*1847G>A	ENSP00000513392.1:n.*1847G>A
ENST00000697681.1:c.*2044G>A	ENSP00000513393.1:n.*2044G>A
ENST00000697683.1:c.*1747G>A	ENSP00000513395.1:n.*1747G>A
ENST00000697684.1:n.943G>A
ENST00000697685.1:c.*1580G>A	ENSP00000513396.1:n.*1580G>A
ENST00000697686.1:c.532G>A	ENSP00000513397.1:p.Ala178Thr
ENST00000697687.1:n.762G>A
ENST00000697688.1:n.929G>A
ENST00000697689.1:c.*1419G>A	ENSP00000513398.1:n.*1419G>A
ENST00000697690.1:c.883G>A	ENSP00000513399.1:p.Ala295Thr
ENST00000697691.1:c.*855G>A	ENSP00000513400.1:n.*855G>A
ENST00000697692.1:c.*895G>A	ENSP00000513401.1:n.*895G>A
ENST00000697694.1:c.532G>A	ENSP00000513402.1:p.Ala178Thr
ENST00000697695.1:n.1490G>A
XM_006722001.2:c.883G>A	XP_006722064.1:p.Ala295Thr
XM_006722001.4:c.883G>A	XP_006722064.1:p.Ala295Thr
XM_006722002.2:c.883G>A	XP_006722065.1:p.Ala295Thr
XM_006722002.4:c.883G>A	XP_006722065.1:p.Ala295Thr
XM_006722004.2:c.532G>A	XP_006722067.1:p.Ala178Thr
XM_006722004.3:c.532G>A	XP_006722067.1:p.Ala178Thr
XM_006722005.2:c.532G>A	XP_006722068.1:p.Ala178Thr
XM_006722005.3:c.532G>A	XP_006722068.1:p.Ala178Thr
XM_011525092.1:c.532G>A	XP_011523394.1:p.Ala178Thr
XM_011525092.2:c.532G>A	XP_011523394.1:p.Ala178Thr
XM_011525093.1:c.532G>A	XP_011523395.1:p.Ala178Thr
XM_011525093.2:c.532G>A	XP_011523395.1:p.Ala178Thr
XM_011525094.1:c.532G>A	XP_011523396.1:p.Ala178Thr
XM_011525094.2:c.532G>A	XP_011523396.1:p.Ala178Thr
XM_017024914.1:c.532G>A	XP_016880403.1:p.Ala178Thr
XM_017024915.1:c.532G>A	XP_016880404.1:p.Ala178Thr
XM_017024916.1:c.532G>A	XP_016880405.1:p.Ala178Thr
XM_017024917.1:c.532G>A	XP_016880406.1:p.Ala178Thr
XM_017024918.2:c.532G>A	XP_016880407.1:p.Ala178Thr
XM_017024919.1:c.532G>A	XP_016880408.1:p.Ala178Thr
XR_934513.1:n.1101G>A
XR_934513.3:n.1532G>A
XR_934514.1:n.1101G>A
XR_934514.3:n.1532G>A