Canonical Allele Identifier: CA3057229509
Community Standard Title: NM_058216.3(RAD51C):c.453_454delinsTT (p.Ala152Ser)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58696741_58696742delinsTT , CM000679.2:g.58696741_58696742delinsTT GRCh38
NC_000017.10:g.56774102_56774103delinsTT , CM000679.1:g.56774102_56774103delinsTT GRCh37
NC_000017.9:g.54129101_54129102delinsTT NCBI36
NG_023199.1:g.9140_9141delinsTT , LRG_314:g.9140_9141delinsTT
NG_047169.1:g.338_339delinsAA

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.453_454delinsTT MANE Select NP_478123.1:p.Ala152Ser
ENST00000337432.9:c.453_454delinsTT MANE Select ENSP00000336701.4:p.Ala152Ser
NM_058216.2:c.453_454delinsTT NP_478123.1:p.Ala152Ser
NR_103872.1:n.475+1552_475+1553delinsTT
NR_103872.2:n.446+1552_446+1553delinsTT
ENST00000337432.8:c.453_454delinsTT ENSP00000336701.4:p.Ala152Ser
ENST00000413590.5:c.91_92delinsTT
ENST00000425173.5:c.249_250delinsTT ENSP00000407282.1:p.Ala84Ser
ENST00000461271.5:c.102_103delinsTT ENSP00000464056.1:p.Ala35Ser
ENST00000461271.6:c.102_103delinsTT ENSP00000464056.2:p.Ala35Ser
ENST00000475762.5:c.*1156_*1157delinsTT ENSP00000432421.1:n.*1156_*1157delinsTT
ENST00000482007.5:c.404+1552_404+1553delinsTT ENSP00000433332.1:n.404+1552_404+1553delinsTT
ENST00000487525.5:c.404+1552_404+1553delinsTT ENSP00000431637.1:n.404+1552_404+1553delinsTT
ENST00000487921.5:n.365_366delinsTT
ENST00000583539.5:c.453_454delinsTT ENSP00000463121.1:p.Ala152Ser
ENST00000584617.5:c.175_176delinsTT
ENST00000622327.4:c.189_190delinsTT ENSP00000482326.1:p.Ala64Ser
ENST00000697675.1:n.3050_3051delinsTT
ENST00000697676.1:n.513_514delinsTT
ENST00000697677.1:n.1534_1535delinsTT
ENST00000697678.1:n.355_356delinsTT
ENST00000697679.1:n.1527_1528delinsTT
ENST00000697680.1:c.*1317_*1318delinsTT ENSP00000513392.1:n.*1317_*1318delinsTT
ENST00000697681.1:c.*1344_*1345delinsTT ENSP00000513393.1:n.*1344_*1345delinsTT
ENST00000697683.1:c.*1317_*1318delinsTT ENSP00000513395.1:n.*1317_*1318delinsTT
ENST00000697684.1:n.513_514delinsTT
ENST00000697685.1:c.*1268+1552_*1268+1553delinsTT ENSP00000513396.1:n.*1268+1552_*1268+1553delinsTT
ENST00000697686.1:c.102_103delinsTT ENSP00000513397.1:p.Ala35Ser
ENST00000697687.1:n.450+1552_450+1553delinsTT
ENST00000697688.1:n.499_500delinsTT
ENST00000697689.1:c.*1107+1552_*1107+1553delinsTT ENSP00000513398.1:n.*1107+1552_*1107+1553delinsTT
ENST00000697690.1:c.453_454delinsTT ENSP00000513399.1:p.Ala152Ser
ENST00000697691.1:c.*425_*426delinsTT ENSP00000513400.1:n.*425_*426delinsTT
ENST00000697692.1:c.*465_*466delinsTT ENSP00000513401.1:n.*465_*466delinsTT
ENST00000697694.1:c.102_103delinsTT ENSP00000513402.1:p.Ala35Ser
ENST00000697695.1:n.1060_1061delinsTT
XM_006722001.2:c.453_454delinsTT XP_006722064.1:p.Ala152Ser
XM_006722001.4:c.453_454delinsTT XP_006722064.1:p.Ala152Ser
XM_006722002.2:c.453_454delinsTT XP_006722065.1:p.Ala152Ser
XM_006722002.4:c.453_454delinsTT XP_006722065.1:p.Ala152Ser
XM_006722004.2:c.102_103delinsTT XP_006722067.1:p.Ala35Ser
XM_006722004.3:c.102_103delinsTT XP_006722067.1:p.Ala35Ser
XM_006722005.2:c.102_103delinsTT XP_006722068.1:p.Ala35Ser
XM_006722005.3:c.102_103delinsTT XP_006722068.1:p.Ala35Ser
XM_011525092.1:c.102_103delinsTT XP_011523394.1:p.Ala35Ser
XM_011525092.2:c.102_103delinsTT XP_011523394.1:p.Ala35Ser
XM_011525093.1:c.102_103delinsTT XP_011523395.1:p.Ala35Ser
XM_011525093.2:c.102_103delinsTT XP_011523395.1:p.Ala35Ser
XM_011525094.1:c.102_103delinsTT XP_011523396.1:p.Ala35Ser
XM_011525094.2:c.102_103delinsTT XP_011523396.1:p.Ala35Ser
XM_017024914.1:c.102_103delinsTT XP_016880403.1:p.Ala35Ser
XM_017024915.1:c.102_103delinsTT XP_016880404.1:p.Ala35Ser
XM_017024916.1:c.102_103delinsTT XP_016880405.1:p.Ala35Ser
XM_017024917.1:c.102_103delinsTT XP_016880406.1:p.Ala35Ser
XM_017024918.2:c.102_103delinsTT XP_016880407.1:p.Ala35Ser
XM_017024919.1:c.102_103delinsTT XP_016880408.1:p.Ala35Ser
XR_934513.1:n.526_527delinsTT
XR_934513.3:n.957_958delinsTT
XR_934514.1:n.526_527delinsTT
XR_934514.3:n.957_958delinsTT