Canonical Allele Identifier: CA3057242897
Community Standard Title: NM_058216.3(RAD51C):c.774_775delinsAG (p.Thr259Ala)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709927_58709928delinsAG , CM000679.2:g.58709927_58709928delinsAG GRCh38
NC_000017.10:g.56787288_56787289delinsAG , CM000679.1:g.56787288_56787289delinsAG GRCh37
NC_000017.9:g.54142287_54142288delinsAG NCBI36
NG_023199.1:g.22326_22327delinsAG , LRG_314:g.22326_22327delinsAG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.774_775delinsAG MANE Select NP_478123.1:p.Thr259Ala
ENST00000337432.9:c.774_775delinsAG MANE Select ENSP00000336701.4:p.Thr259Ala
NM_058216.2:c.774_775delinsAG NP_478123.1:p.Thr259Ala
NR_103872.1:n.678_679delinsAG
NR_103872.2:n.649_650delinsAG
ENST00000337432.8:c.774_775delinsAG ENSP00000336701.4:p.Thr259Ala
ENST00000413590.5:c.412_413delinsAG
ENST00000461271.6:c.423_424delinsAG ENSP00000464056.2:p.Thr142Ala
ENST00000475762.5:c.*1477_*1478delinsAG ENSP00000432421.1:n.*1477_*1478delinsAG
ENST00000482007.5:c.*202_*203delinsAG ENSP00000433332.1:n.*202_*203delinsAG
ENST00000487525.5:c.*347_*348delinsAG ENSP00000431637.1:n.*347_*348delinsAG
ENST00000578151.1:n.109_110delinsAG
ENST00000581221.5:n.289_290delinsAG
ENST00000583539.5:c.774_775delinsAG ENSP00000463121.1:p.Thr259Ala
ENST00000584617.5:c.496_497delinsAG
ENST00000584804.1:c.69_70delinsAG ENSP00000463658.1:p.Thr24Ala
ENST00000697678.1:n.676_677delinsAG
ENST00000697679.1:n.1848_1849delinsAG
ENST00000697680.1:c.*1638_*1639delinsAG ENSP00000513392.1:n.*1638_*1639delinsAG
ENST00000697681.1:c.*1935_*1936delinsAG ENSP00000513393.1:n.*1935_*1936delinsAG
ENST00000697683.1:c.*1638_*1639delinsAG ENSP00000513395.1:n.*1638_*1639delinsAG
ENST00000697684.1:n.834_835delinsAG
ENST00000697685.1:c.*1471_*1472delinsAG ENSP00000513396.1:n.*1471_*1472delinsAG
ENST00000697686.1:c.423_424delinsAG ENSP00000513397.1:p.Thr142Ala
ENST00000697687.1:n.653_654delinsAG
ENST00000697688.1:n.820_821delinsAG
ENST00000697689.1:c.*1310_*1311delinsAG ENSP00000513398.1:n.*1310_*1311delinsAG
ENST00000697690.1:c.774_775delinsAG ENSP00000513399.1:p.Thr259Ala
ENST00000697691.1:c.*746_*747delinsAG ENSP00000513400.1:n.*746_*747delinsAG
ENST00000697692.1:c.*786_*787delinsAG ENSP00000513401.1:n.*786_*787delinsAG
ENST00000697694.1:c.423_424delinsAG ENSP00000513402.1:p.Thr142Ala
ENST00000697695.1:n.1381_1382delinsAG
XM_006722001.2:c.774_775delinsAG XP_006722064.1:p.Thr259Ala
XM_006722001.4:c.774_775delinsAG XP_006722064.1:p.Thr259Ala
XM_006722002.2:c.774_775delinsAG XP_006722065.1:p.Thr259Ala
XM_006722002.4:c.774_775delinsAG XP_006722065.1:p.Thr259Ala
XM_006722004.2:c.423_424delinsAG XP_006722067.1:p.Thr142Ala
XM_006722004.3:c.423_424delinsAG XP_006722067.1:p.Thr142Ala
XM_006722005.2:c.423_424delinsAG XP_006722068.1:p.Thr142Ala
XM_006722005.3:c.423_424delinsAG XP_006722068.1:p.Thr142Ala
XM_011525092.1:c.423_424delinsAG XP_011523394.1:p.Thr142Ala
XM_011525092.2:c.423_424delinsAG XP_011523394.1:p.Thr142Ala
XM_011525093.1:c.423_424delinsAG XP_011523395.1:p.Thr142Ala
XM_011525093.2:c.423_424delinsAG XP_011523395.1:p.Thr142Ala
XM_011525094.1:c.423_424delinsAG XP_011523396.1:p.Thr142Ala
XM_011525094.2:c.423_424delinsAG XP_011523396.1:p.Thr142Ala
XM_017024914.1:c.423_424delinsAG XP_016880403.1:p.Thr142Ala
XM_017024915.1:c.423_424delinsAG XP_016880404.1:p.Thr142Ala
XM_017024916.1:c.423_424delinsAG XP_016880405.1:p.Thr142Ala
XM_017024917.1:c.423_424delinsAG XP_016880406.1:p.Thr142Ala
XM_017024918.2:c.423_424delinsAG XP_016880407.1:p.Thr142Ala
XM_017024919.1:c.423_424delinsAG XP_016880408.1:p.Thr142Ala
XR_934513.1:n.992_993delinsAG
XR_934513.3:n.1423_1424delinsAG
XR_934514.1:n.992_993delinsAG
XR_934514.3:n.1423_1424delinsAG