Canonical Allele Identifier: CA3057229593
Community Standard Title: NM_058216.3(RAD51C):c.519_520delinsCG (p.Thr174Ala)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58696807_58696808delinsCG , CM000679.2:g.58696807_58696808delinsCG GRCh38
NC_000017.10:g.56774168_56774169delinsCG , CM000679.1:g.56774168_56774169delinsCG GRCh37
NC_000017.9:g.54129167_54129168delinsCG NCBI36
NG_023199.1:g.9206_9207delinsCG , LRG_314:g.9206_9207delinsCG
NG_047169.1:g.272_273delinsCG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.519_520delinsCG MANE Select NP_478123.1:p.Thr174Ala
ENST00000337432.9:c.519_520delinsCG MANE Select ENSP00000336701.4:p.Thr174Ala
NM_058216.2:c.519_520delinsCG NP_478123.1:p.Thr174Ala
NR_103872.1:n.475+1618_475+1619delinsCG
NR_103872.2:n.446+1618_446+1619delinsCG
ENST00000337432.8:c.519_520delinsCG ENSP00000336701.4:p.Thr174Ala
ENST00000413590.5:c.157_158delinsCG
ENST00000425173.5:c.315_316delinsCG ENSP00000407282.1:p.Thr106Ala
ENST00000461271.5:c.168_169delinsCG ENSP00000464056.1:p.Thr57Ala
ENST00000461271.6:c.168_169delinsCG ENSP00000464056.2:p.Thr57Ala
ENST00000475762.5:c.*1222_*1223delinsCG ENSP00000432421.1:n.*1222_*1223delinsCG
ENST00000482007.5:c.404+1618_404+1619delinsCG ENSP00000433332.1:n.404+1618_404+1619delinsCG
ENST00000487525.5:c.404+1618_404+1619delinsCG ENSP00000431637.1:n.404+1618_404+1619delinsCG
ENST00000487921.5:n.431_432delinsCG
ENST00000583539.5:c.519_520delinsCG ENSP00000463121.1:p.Thr174Ala
ENST00000584617.5:c.241_242delinsCG
ENST00000622327.4:c.255_256delinsCG ENSP00000482326.1:p.Thr86Ala
ENST00000697675.1:n.3116_3117delinsCG
ENST00000697676.1:n.579_580delinsCG
ENST00000697677.1:n.1600_1601delinsCG
ENST00000697678.1:n.421_422delinsCG
ENST00000697679.1:n.1593_1594delinsCG
ENST00000697680.1:c.*1383_*1384delinsCG ENSP00000513392.1:n.*1383_*1384delinsCG
ENST00000697681.1:c.*1410_*1411delinsCG ENSP00000513393.1:n.*1410_*1411delinsCG
ENST00000697683.1:c.*1383_*1384delinsCG ENSP00000513395.1:n.*1383_*1384delinsCG
ENST00000697684.1:n.579_580delinsCG
ENST00000697685.1:c.*1268+1618_*1268+1619delinsCG ENSP00000513396.1:n.*1268+1618_*1268+1619delinsCG
ENST00000697686.1:c.168_169delinsCG ENSP00000513397.1:p.Thr57Ala
ENST00000697687.1:n.450+1618_450+1619delinsCG
ENST00000697688.1:n.565_566delinsCG
ENST00000697689.1:c.*1107+1618_*1107+1619delinsCG ENSP00000513398.1:n.*1107+1618_*1107+1619delinsCG
ENST00000697690.1:c.519_520delinsCG ENSP00000513399.1:p.Thr174Ala
ENST00000697691.1:c.*491_*492delinsCG ENSP00000513400.1:n.*491_*492delinsCG
ENST00000697692.1:c.*531_*532delinsCG ENSP00000513401.1:n.*531_*532delinsCG
ENST00000697694.1:c.168_169delinsCG ENSP00000513402.1:p.Thr57Ala
ENST00000697695.1:n.1126_1127delinsCG
XM_006722001.2:c.519_520delinsCG XP_006722064.1:p.Thr174Ala
XM_006722001.4:c.519_520delinsCG XP_006722064.1:p.Thr174Ala
XM_006722002.2:c.519_520delinsCG XP_006722065.1:p.Thr174Ala
XM_006722002.4:c.519_520delinsCG XP_006722065.1:p.Thr174Ala
XM_006722004.2:c.168_169delinsCG XP_006722067.1:p.Thr57Ala
XM_006722004.3:c.168_169delinsCG XP_006722067.1:p.Thr57Ala
XM_006722005.2:c.168_169delinsCG XP_006722068.1:p.Thr57Ala
XM_006722005.3:c.168_169delinsCG XP_006722068.1:p.Thr57Ala
XM_011525092.1:c.168_169delinsCG XP_011523394.1:p.Thr57Ala
XM_011525092.2:c.168_169delinsCG XP_011523394.1:p.Thr57Ala
XM_011525093.1:c.168_169delinsCG XP_011523395.1:p.Thr57Ala
XM_011525093.2:c.168_169delinsCG XP_011523395.1:p.Thr57Ala
XM_011525094.1:c.168_169delinsCG XP_011523396.1:p.Thr57Ala
XM_011525094.2:c.168_169delinsCG XP_011523396.1:p.Thr57Ala
XM_017024914.1:c.168_169delinsCG XP_016880403.1:p.Thr57Ala
XM_017024915.1:c.168_169delinsCG XP_016880404.1:p.Thr57Ala
XM_017024916.1:c.168_169delinsCG XP_016880405.1:p.Thr57Ala
XM_017024917.1:c.168_169delinsCG XP_016880406.1:p.Thr57Ala
XM_017024918.2:c.168_169delinsCG XP_016880407.1:p.Thr57Ala
XM_017024919.1:c.168_169delinsCG XP_016880408.1:p.Thr57Ala
XR_934513.1:n.592_593delinsCG
XR_934513.3:n.1023_1024delinsCG
XR_934514.1:n.592_593delinsCG
XR_934514.3:n.1023_1024delinsCG