Canonical Allele Identifier: CA3057229597
Community Standard Title: NM_058216.3(RAD51C):c.523_524delinsAG (p.Ala175Ser)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58696811_58696812delinsAG , CM000679.2:g.58696811_58696812delinsAG GRCh38
NC_000017.10:g.56774172_56774173delinsAG , CM000679.1:g.56774172_56774173delinsAG GRCh37
NC_000017.9:g.54129171_54129172delinsAG NCBI36
NG_023199.1:g.9210_9211delinsAG , LRG_314:g.9210_9211delinsAG
NG_047169.1:g.268_269delinsCT

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.523_524delinsAG MANE Select NP_478123.1:p.Ala175Ser
ENST00000337432.9:c.523_524delinsAG MANE Select ENSP00000336701.4:p.Ala175Ser
NM_058216.2:c.523_524delinsAG NP_478123.1:p.Ala175Ser
NR_103872.1:n.475+1622_475+1623delinsAG
NR_103872.2:n.446+1622_446+1623delinsAG
ENST00000337432.8:c.523_524delinsAG ENSP00000336701.4:p.Ala175Ser
ENST00000413590.5:c.161_162delinsAG
ENST00000425173.5:c.319_320delinsAG ENSP00000407282.1:p.Ala107Ser
ENST00000461271.5:c.172_173delinsAG ENSP00000464056.1:p.Ala58Ser
ENST00000461271.6:c.172_173delinsAG ENSP00000464056.2:p.Ala58Ser
ENST00000475762.5:c.*1226_*1227delinsAG ENSP00000432421.1:n.*1226_*1227delinsAG
ENST00000482007.5:c.404+1622_404+1623delinsAG ENSP00000433332.1:n.404+1622_404+1623delinsAG
ENST00000487525.5:c.404+1622_404+1623delinsAG ENSP00000431637.1:n.404+1622_404+1623delinsAG
ENST00000487921.5:n.435_436delinsAG
ENST00000583539.5:c.523_524delinsAG ENSP00000463121.1:p.Ala175Ser
ENST00000584617.5:c.245_246delinsAG
ENST00000622327.4:c.259_260delinsAG ENSP00000482326.1:p.Ala87Ser
ENST00000697675.1:n.3120_3121delinsAG
ENST00000697676.1:n.583_584delinsAG
ENST00000697677.1:n.1604_1605delinsAG
ENST00000697678.1:n.425_426delinsAG
ENST00000697679.1:n.1597_1598delinsAG
ENST00000697680.1:c.*1387_*1388delinsAG ENSP00000513392.1:n.*1387_*1388delinsAG
ENST00000697681.1:c.*1414_*1415delinsAG ENSP00000513393.1:n.*1414_*1415delinsAG
ENST00000697683.1:c.*1387_*1388delinsAG ENSP00000513395.1:n.*1387_*1388delinsAG
ENST00000697684.1:n.583_584delinsAG
ENST00000697685.1:c.*1268+1622_*1268+1623delinsAG ENSP00000513396.1:n.*1268+1622_*1268+1623delinsAG
ENST00000697686.1:c.172_173delinsAG ENSP00000513397.1:p.Ala58Ser
ENST00000697687.1:n.450+1622_450+1623delinsAG
ENST00000697688.1:n.569_570delinsAG
ENST00000697689.1:c.*1107+1622_*1107+1623delinsAG ENSP00000513398.1:n.*1107+1622_*1107+1623delinsAG
ENST00000697690.1:c.523_524delinsAG ENSP00000513399.1:p.Ala175Ser
ENST00000697691.1:c.*495_*496delinsAG ENSP00000513400.1:n.*495_*496delinsAG
ENST00000697692.1:c.*535_*536delinsAG ENSP00000513401.1:n.*535_*536delinsAG
ENST00000697694.1:c.172_173delinsAG ENSP00000513402.1:p.Ala58Ser
ENST00000697695.1:n.1130_1131delinsAG
XM_006722001.2:c.523_524delinsAG XP_006722064.1:p.Ala175Ser
XM_006722001.4:c.523_524delinsAG XP_006722064.1:p.Ala175Ser
XM_006722002.2:c.523_524delinsAG XP_006722065.1:p.Ala175Ser
XM_006722002.4:c.523_524delinsAG XP_006722065.1:p.Ala175Ser
XM_006722004.2:c.172_173delinsAG XP_006722067.1:p.Ala58Ser
XM_006722004.3:c.172_173delinsAG XP_006722067.1:p.Ala58Ser
XM_006722005.2:c.172_173delinsAG XP_006722068.1:p.Ala58Ser
XM_006722005.3:c.172_173delinsAG XP_006722068.1:p.Ala58Ser
XM_011525092.1:c.172_173delinsAG XP_011523394.1:p.Ala58Ser
XM_011525092.2:c.172_173delinsAG XP_011523394.1:p.Ala58Ser
XM_011525093.1:c.172_173delinsAG XP_011523395.1:p.Ala58Ser
XM_011525093.2:c.172_173delinsAG XP_011523395.1:p.Ala58Ser
XM_011525094.1:c.172_173delinsAG XP_011523396.1:p.Ala58Ser
XM_011525094.2:c.172_173delinsAG XP_011523396.1:p.Ala58Ser
XM_017024914.1:c.172_173delinsAG XP_016880403.1:p.Ala58Ser
XM_017024915.1:c.172_173delinsAG XP_016880404.1:p.Ala58Ser
XM_017024916.1:c.172_173delinsAG XP_016880405.1:p.Ala58Ser
XM_017024917.1:c.172_173delinsAG XP_016880406.1:p.Ala58Ser
XM_017024918.2:c.172_173delinsAG XP_016880407.1:p.Ala58Ser
XM_017024919.1:c.172_173delinsAG XP_016880408.1:p.Ala58Ser
XR_934513.1:n.596_597delinsAG
XR_934513.3:n.1027_1028delinsAG
XR_934514.1:n.596_597delinsAG
XR_934514.3:n.1027_1028delinsAG