Canonical Allele Identifier: CA400359719

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58720792C>G , CM000679.2:g.58720792C>G	GRCh38
NC_000017.10:g.56798153C>G , CM000679.1:g.56798153C>G	GRCh37
NC_000017.9:g.54153152C>G	NCBI36
NG_023199.1:g.33191C>G , LRG_314:g.33191C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_058216.3:c.884C>G MANE Select	NP_478123.1:p.Ala295Gly
ENST00000337432.9:c.884C>G MANE Select	ENSP00000336701.4:p.Ala295Gly
NM_058216.2:c.884C>G	NP_478123.1:p.Ala295Gly
NR_103872.1:n.788C>G
NR_103872.2:n.759C>G
ENST00000337432.8:c.884C>G	ENSP00000336701.4:p.Ala295Gly
ENST00000413590.5:c.522C>G
ENST00000461271.6:c.533C>G	ENSP00000464056.2:p.Ala178Gly
ENST00000475762.5:c.*1541-3248C>G	ENSP00000432421.1:n.*1541-3248C>G
ENST00000482007.5:c.*312C>G	ENSP00000433332.1:n.*312C>G
ENST00000487525.5:c.*457C>G	ENSP00000431637.1:n.*457C>G
ENST00000578151.1:n.219C>G
ENST00000581221.5:n.399C>G
ENST00000583539.5:c.884C>G	ENSP00000463121.1:p.Ala295Gly
ENST00000584617.5:c.606C>G
ENST00000584804.1:c.179C>G	ENSP00000463658.1:p.Ala60Gly
ENST00000697678.1:n.786C>G
ENST00000697679.1:n.1958C>G
ENST00000697680.1:c.*1848C>G	ENSP00000513392.1:n.*1848C>G
ENST00000697681.1:c.*2045C>G	ENSP00000513393.1:n.*2045C>G
ENST00000697683.1:c.*1748C>G	ENSP00000513395.1:n.*1748C>G
ENST00000697684.1:n.944C>G
ENST00000697685.1:c.*1581C>G	ENSP00000513396.1:n.*1581C>G
ENST00000697686.1:c.533C>G	ENSP00000513397.1:p.Ala178Gly
ENST00000697687.1:n.763C>G
ENST00000697688.1:n.930C>G
ENST00000697689.1:c.*1420C>G	ENSP00000513398.1:n.*1420C>G
ENST00000697690.1:c.884C>G	ENSP00000513399.1:p.Ala295Gly
ENST00000697691.1:c.*856C>G	ENSP00000513400.1:n.*856C>G
ENST00000697692.1:c.*896C>G	ENSP00000513401.1:n.*896C>G
ENST00000697694.1:c.533C>G	ENSP00000513402.1:p.Ala178Gly
ENST00000697695.1:n.1491C>G
XM_006722001.2:c.884C>G	XP_006722064.1:p.Ala295Gly
XM_006722001.4:c.884C>G	XP_006722064.1:p.Ala295Gly
XM_006722002.2:c.884C>G	XP_006722065.1:p.Ala295Gly
XM_006722002.4:c.884C>G	XP_006722065.1:p.Ala295Gly
XM_006722004.2:c.533C>G	XP_006722067.1:p.Ala178Gly
XM_006722004.3:c.533C>G	XP_006722067.1:p.Ala178Gly
XM_006722005.2:c.533C>G	XP_006722068.1:p.Ala178Gly
XM_006722005.3:c.533C>G	XP_006722068.1:p.Ala178Gly
XM_011525092.1:c.533C>G	XP_011523394.1:p.Ala178Gly
XM_011525092.2:c.533C>G	XP_011523394.1:p.Ala178Gly
XM_011525093.1:c.533C>G	XP_011523395.1:p.Ala178Gly
XM_011525093.2:c.533C>G	XP_011523395.1:p.Ala178Gly
XM_011525094.1:c.533C>G	XP_011523396.1:p.Ala178Gly
XM_011525094.2:c.533C>G	XP_011523396.1:p.Ala178Gly
XM_017024914.1:c.533C>G	XP_016880403.1:p.Ala178Gly
XM_017024915.1:c.533C>G	XP_016880404.1:p.Ala178Gly
XM_017024916.1:c.533C>G	XP_016880405.1:p.Ala178Gly
XM_017024917.1:c.533C>G	XP_016880406.1:p.Ala178Gly
XM_017024918.2:c.533C>G	XP_016880407.1:p.Ala178Gly
XM_017024919.1:c.533C>G	XP_016880408.1:p.Ala178Gly
XR_934513.1:n.1102C>G
XR_934513.3:n.1533C>G
XR_934514.1:n.1102C>G
XR_934514.3:n.1533C>G