Canonical Allele Identifier: CA3057243450
Community Standard Title: NM_058216.3(RAD51C):c.1003_1004delinsGC (p.Cys335Ala)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732521_58732522delinsGC , CM000679.2:g.58732521_58732522delinsGC GRCh38
NC_000017.10:g.56809882_56809883delinsGC , CM000679.1:g.56809882_56809883delinsGC GRCh37
NC_000017.9:g.54164881_54164882delinsGC NCBI36
NG_023199.1:g.44920_44921delinsGC , LRG_314:g.44920_44921delinsGC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1003_1004delinsGC MANE Select NP_478123.1:p.Cys335Ala
ENST00000337432.9:c.1003_1004delinsGC MANE Select ENSP00000336701.4:p.Cys335Ala
NM_058216.2:c.1003_1004delinsGC NP_478123.1:p.Cys335Ala
NR_103872.1:n.907_908delinsGC
NR_103872.2:n.878_879delinsGC
ENST00000337432.8:c.1003_1004delinsGC ENSP00000336701.4:p.Cys335Ala
ENST00000413590.5:c.644_645delinsGC
ENST00000461271.6:c.652_653delinsGC ENSP00000464056.2:p.Cys218Ala
ENST00000461706.1:n.190_191delinsGC
ENST00000475762.5:c.*1639_*1640delinsGC ENSP00000432421.1:n.*1639_*1640delinsGC
ENST00000482007.5:c.*431_*432delinsGC ENSP00000433332.1:n.*431_*432delinsGC
ENST00000487525.5:c.*579_*580delinsGC ENSP00000431637.1:n.*579_*580delinsGC
ENST00000578151.1:n.240-1597_240-1596delinsGC
ENST00000581221.5:n.518_519delinsGC
ENST00000583539.5:c.1003_1004delinsGC ENSP00000463121.1:p.Cys335Ala
ENST00000584804.1:c.237_238delinsGC ENSP00000463658.1:p.Asn79_Ala80delinsLysPro
ENST00000697680.1:c.*1967_*1968delinsGC ENSP00000513392.1:n.*1967_*1968delinsGC
ENST00000697681.1:c.*2164_*2165delinsGC ENSP00000513393.1:n.*2164_*2165delinsGC
ENST00000697683.1:c.*1939_*1940delinsGC ENSP00000513395.1:n.*1939_*1940delinsGC
ENST00000697685.1:c.*1700_*1701delinsGC ENSP00000513396.1:n.*1700_*1701delinsGC
ENST00000697686.1:c.774_775delinsGC ENSP00000513397.1:p.Asn258_Ala259delinsLysPro
ENST00000697689.1:c.*1441-1597_*1441-1596delinsGC ENSP00000513398.1:n.*1441-1597_*1441-1596delinsGC
ENST00000697690.1:c.905-1597_905-1596delinsGC ENSP00000513399.1:n.905-1597_905-1596delinsGC
ENST00000697691.1:c.*975_*976delinsGC ENSP00000513400.1:n.*975_*976delinsGC
ENST00000697692.1:c.*1015_*1016delinsGC ENSP00000513401.1:n.*1015_*1016delinsGC
ENST00000697694.1:c.652_653delinsGC ENSP00000513402.1:p.Cys218Ala
ENST00000697695.1:n.1610_1611delinsGC
XM_006722001.2:c.1006_1007delinsGC XP_006722064.1:p.Cys336Ala
XM_006722001.4:c.1006_1007delinsGC XP_006722064.1:p.Cys336Ala
XM_006722002.2:c.942_943delinsGC XP_006722065.1:p.Asn314_Ala315delinsLysPro
XM_006722002.4:c.942_943delinsGC XP_006722065.1:p.Asn314_Ala315delinsLysPro
XM_006722004.2:c.655_656delinsGC XP_006722067.1:p.Cys219Ala
XM_006722004.3:c.655_656delinsGC XP_006722067.1:p.Cys219Ala
XM_006722005.2:c.655_656delinsGC XP_006722068.1:p.Cys219Ala
XM_006722005.3:c.655_656delinsGC XP_006722068.1:p.Cys219Ala
XM_011525092.1:c.655_656delinsGC XP_011523394.1:p.Cys219Ala
XM_011525092.2:c.655_656delinsGC XP_011523394.1:p.Cys219Ala
XM_011525093.1:c.655_656delinsGC XP_011523395.1:p.Cys219Ala
XM_011525093.2:c.655_656delinsGC XP_011523395.1:p.Cys219Ala
XM_011525094.1:c.655_656delinsGC XP_011523396.1:p.Cys219Ala
XM_011525094.2:c.655_656delinsGC XP_011523396.1:p.Cys219Ala
XM_017024914.1:c.652_653delinsGC XP_016880403.1:p.Cys218Ala
XM_017024915.1:c.652_653delinsGC XP_016880404.1:p.Cys218Ala
XM_017024916.1:c.652_653delinsGC XP_016880405.1:p.Cys218Ala
XM_017024917.1:c.652_653delinsGC XP_016880406.1:p.Cys218Ala
XM_017024918.2:c.652_653delinsGC XP_016880407.1:p.Cys218Ala
XM_017024919.1:c.591_592delinsGC XP_016880408.1:p.Asn197_Ala198delinsLysPro
XR_934513.1:n.1221_1222delinsGC
XR_934513.3:n.1652_1653delinsGC
XR_934514.1:n.1224_1225delinsGC
XR_934514.3:n.1655_1656delinsGC
XR_934886.1:n.149+5549_149+5550delinsGC
XR_934886.2:n.149+5549_149+5550delinsGC