Canonical Allele Identifier: CA3261178920
Community Standard Title: NM_058216.3(RAD51C):c.872_873delinsTG (p.Asp291Val)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58720780_58720781delinsTG , CM000679.2:g.58720780_58720781delinsTG GRCh38
NC_000017.10:g.56798141_56798142delinsTG , CM000679.1:g.56798141_56798142delinsTG GRCh37
NC_000017.9:g.54153140_54153141delinsTG NCBI36
NG_023199.1:g.33179_33180delinsTG , LRG_314:g.33179_33180delinsTG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.872_873delinsTG MANE Select NP_478123.1:p.Asp291Val
ENST00000337432.9:c.872_873delinsTG MANE Select ENSP00000336701.4:p.Asp291Val
NM_058216.2:c.872_873delinsTG NP_478123.1:p.Asp291Val
NR_103872.1:n.776_777delinsTG
NR_103872.2:n.747_748delinsTG
ENST00000337432.8:c.872_873delinsTG ENSP00000336701.4:p.Asp291Val
ENST00000413590.5:c.510_511delinsTG
ENST00000461271.6:c.521_522delinsTG ENSP00000464056.2:p.Asp174Val
ENST00000475762.5:c.*1541-3260_*1541-3259delinsTG ENSP00000432421.1:n.*1541-3260_*1541-3259delinsTG
ENST00000482007.5:c.*300_*301delinsTG ENSP00000433332.1:n.*300_*301delinsTG
ENST00000487525.5:c.*445_*446delinsTG ENSP00000431637.1:n.*445_*446delinsTG
ENST00000578151.1:n.207_208delinsTG
ENST00000581221.5:n.387_388delinsTG
ENST00000583539.5:c.872_873delinsTG ENSP00000463121.1:p.Asp291Val
ENST00000584617.5:c.594_595delinsTG
ENST00000584804.1:c.167_168delinsTG ENSP00000463658.1:p.Asp56Val
ENST00000697678.1:n.774_775delinsTG
ENST00000697679.1:n.1946_1947delinsTG
ENST00000697680.1:c.*1836_*1837delinsTG ENSP00000513392.1:n.*1836_*1837delinsTG
ENST00000697681.1:c.*2033_*2034delinsTG ENSP00000513393.1:n.*2033_*2034delinsTG
ENST00000697683.1:c.*1736_*1737delinsTG ENSP00000513395.1:n.*1736_*1737delinsTG
ENST00000697684.1:n.932_933delinsTG
ENST00000697685.1:c.*1569_*1570delinsTG ENSP00000513396.1:n.*1569_*1570delinsTG
ENST00000697686.1:c.521_522delinsTG ENSP00000513397.1:p.Asp174Val
ENST00000697687.1:n.751_752delinsTG
ENST00000697688.1:n.918_919delinsTG
ENST00000697689.1:c.*1408_*1409delinsTG ENSP00000513398.1:n.*1408_*1409delinsTG
ENST00000697690.1:c.872_873delinsTG ENSP00000513399.1:p.Asp291Val
ENST00000697691.1:c.*844_*845delinsTG ENSP00000513400.1:n.*844_*845delinsTG
ENST00000697692.1:c.*884_*885delinsTG ENSP00000513401.1:n.*884_*885delinsTG
ENST00000697694.1:c.521_522delinsTG ENSP00000513402.1:p.Asp174Val
ENST00000697695.1:n.1479_1480delinsTG
XM_006722001.2:c.872_873delinsTG XP_006722064.1:p.Asp291Val
XM_006722001.4:c.872_873delinsTG XP_006722064.1:p.Asp291Val
XM_006722002.2:c.872_873delinsTG XP_006722065.1:p.Asp291Val
XM_006722002.4:c.872_873delinsTG XP_006722065.1:p.Asp291Val
XM_006722004.2:c.521_522delinsTG XP_006722067.1:p.Asp174Val
XM_006722004.3:c.521_522delinsTG XP_006722067.1:p.Asp174Val
XM_006722005.2:c.521_522delinsTG XP_006722068.1:p.Asp174Val
XM_006722005.3:c.521_522delinsTG XP_006722068.1:p.Asp174Val
XM_011525092.1:c.521_522delinsTG XP_011523394.1:p.Asp174Val
XM_011525092.2:c.521_522delinsTG XP_011523394.1:p.Asp174Val
XM_011525093.1:c.521_522delinsTG XP_011523395.1:p.Asp174Val
XM_011525093.2:c.521_522delinsTG XP_011523395.1:p.Asp174Val
XM_011525094.1:c.521_522delinsTG XP_011523396.1:p.Asp174Val
XM_011525094.2:c.521_522delinsTG XP_011523396.1:p.Asp174Val
XM_017024914.1:c.521_522delinsTG XP_016880403.1:p.Asp174Val
XM_017024915.1:c.521_522delinsTG XP_016880404.1:p.Asp174Val
XM_017024916.1:c.521_522delinsTG XP_016880405.1:p.Asp174Val
XM_017024917.1:c.521_522delinsTG XP_016880406.1:p.Asp174Val
XM_017024918.2:c.521_522delinsTG XP_016880407.1:p.Asp174Val
XM_017024919.1:c.521_522delinsTG XP_016880408.1:p.Asp174Val
XR_934513.1:n.1090_1091delinsTG
XR_934513.3:n.1521_1522delinsTG
XR_934514.1:n.1090_1091delinsTG
XR_934514.3:n.1521_1522delinsTG