Canonical Allele Identifier: CA400339634

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58694948G>A , CM000679.2:g.58694948G>A	GRCh38
NC_000017.10:g.56772309G>A , CM000679.1:g.56772309G>A	GRCh37
NC_000017.9:g.54127308G>A	NCBI36
NG_023199.1:g.7347G>A , LRG_314:g.7347G>A
NG_047169.1:g.2132C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_058216.3:c.163G>A MANE Select	NP_478123.1:p.Ala55Thr
ENST00000337432.9:c.163G>A MANE Select	ENSP00000336701.4:p.Ala55Thr
NM_002876.3:c.163G>A	NP_002867.1:p.Ala55Thr
NM_002876.4:c.163G>A	NP_002867.1:p.Ala55Thr
NM_058216.2:c.163G>A	NP_478123.1:p.Ala55Thr
NR_103872.1:n.234G>A
NR_103872.2:n.205G>A
NR_103873.1:n.131G>A
ENST00000337432.8:c.163G>A	ENSP00000336701.4:p.Ala55Thr
ENST00000421782.3:c.163G>A	ENSP00000391450.2:p.Ala55Thr
ENST00000461271.5:c.-189G>A	ENSP00000464056.1:n.-189G>A
ENST00000461271.6:c.-189G>A	ENSP00000464056.2:n.-189G>A
ENST00000475762.5:c.*866G>A	ENSP00000432421.1:n.*866G>A
ENST00000482007.5:c.163G>A	ENSP00000433332.1:p.Ala55Thr
ENST00000486827.1:c.*1027G>A	ENSP00000436761.1:n.*1027G>A
ENST00000487525.5:c.163G>A	ENSP00000431637.1:p.Ala55Thr
ENST00000487921.5:n.75G>A
ENST00000583539.5:c.163G>A	ENSP00000463121.1:p.Ala55Thr
ENST00000584617.5:c.127-1745G>A
ENST00000697675.1:n.1257G>A
ENST00000697676.1:n.223G>A
ENST00000697677.1:n.1244G>A
ENST00000697678.1:n.65G>A
ENST00000697679.1:n.1237G>A
ENST00000697680.1:c.*1027G>A	ENSP00000513392.1:n.*1027G>A
ENST00000697681.1:c.*1027G>A	ENSP00000513393.1:n.*1027G>A
ENST00000697683.1:c.*1027G>A	ENSP00000513395.1:n.*1027G>A
ENST00000697684.1:n.223G>A
ENST00000697685.1:c.*1027G>A	ENSP00000513396.1:n.*1027G>A
ENST00000697686.1:c.-189G>A	ENSP00000513397.1:n.-189G>A
ENST00000697687.1:n.209G>A
ENST00000697688.1:n.209G>A
ENST00000697689.1:c.*866G>A	ENSP00000513398.1:n.*866G>A
ENST00000697690.1:c.163G>A	ENSP00000513399.1:p.Ala55Thr
ENST00000697691.1:c.*135G>A	ENSP00000513400.1:n.*135G>A
ENST00000697692.1:c.*175G>A	ENSP00000513401.1:n.*175G>A
ENST00000697693.1:n.938G>A
ENST00000697694.1:c.-189G>A	ENSP00000513402.1:n.-189G>A
ENST00000697695.1:n.770G>A
XM_006722001.2:c.163G>A	XP_006722064.1:p.Ala55Thr
XM_006722001.4:c.163G>A	XP_006722064.1:p.Ala55Thr
XM_006722002.2:c.163G>A	XP_006722065.1:p.Ala55Thr
XM_006722002.4:c.163G>A	XP_006722065.1:p.Ala55Thr
XM_006722004.2:c.-189G>A	XP_006722067.1:n.-189G>A
XM_006722004.3:c.-189G>A	XP_006722067.1:n.-189G>A
XM_006722005.2:c.-189G>A	XP_006722068.1:n.-189G>A
XM_006722005.3:c.-189G>A	XP_006722068.1:n.-189G>A
XM_011525092.1:c.-189G>A	XP_011523394.1:n.-189G>A
XM_011525092.2:c.-189G>A	XP_011523394.1:n.-189G>A
XM_011525093.1:c.-189G>A	XP_011523395.1:n.-189G>A
XM_011525093.2:c.-189G>A	XP_011523395.1:n.-189G>A
XM_011525094.1:c.-189G>A	XP_011523396.1:n.-189G>A
XM_011525094.2:c.-189G>A	XP_011523396.1:n.-189G>A
XM_017024914.1:c.-189G>A	XP_016880403.1:n.-189G>A
XM_017024915.1:c.-189G>A	XP_016880404.1:n.-189G>A
XM_017024916.1:c.-189G>A	XP_016880405.1:n.-189G>A
XM_017024917.1:c.-189G>A	XP_016880406.1:n.-189G>A
XM_017024918.2:c.-189G>A	XP_016880407.1:n.-189G>A
XM_017024919.1:c.-189G>A	XP_016880408.1:n.-189G>A
XR_934513.1:n.236G>A
XR_934513.3:n.667G>A
XR_934514.1:n.236G>A
XR_934514.3:n.667G>A