Canonical Allele Identifier: CA3057242460
Community Standard Title: NM_058216.3(RAD51C):c.597_598delinsTG (p.Thr200Ala)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703221_58703222delinsTG , CM000679.2:g.58703221_58703222delinsTG GRCh38
NC_000017.10:g.56780582_56780583delinsTG , CM000679.1:g.56780582_56780583delinsTG GRCh37
NC_000017.9:g.54135581_54135582delinsTG NCBI36
NG_023199.1:g.15620_15621delinsTG , LRG_314:g.15620_15621delinsTG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.597_598delinsTG MANE Select NP_478123.1:p.Thr200Ala
ENST00000337432.9:c.597_598delinsTG MANE Select ENSP00000336701.4:p.Thr200Ala
NM_058216.2:c.597_598delinsTG NP_478123.1:p.Thr200Ala
NR_103872.1:n.501_502delinsTG
NR_103872.2:n.472_473delinsTG
ENST00000337432.8:c.597_598delinsTG ENSP00000336701.4:p.Thr200Ala
ENST00000413590.5:c.235_236delinsTG
ENST00000425173.5:c.393_394delinsTG ENSP00000407282.1:p.Thr132Ala
ENST00000461271.5:c.246_247delinsTG ENSP00000464056.1:p.Thr83Ala
ENST00000461271.6:c.246_247delinsTG ENSP00000464056.2:p.Thr83Ala
ENST00000475762.5:c.*1300_*1301delinsTG ENSP00000432421.1:n.*1300_*1301delinsTG
ENST00000482007.5:c.*25_*26delinsTG ENSP00000433332.1:n.*25_*26delinsTG
ENST00000487525.5:c.*25_*26delinsTG ENSP00000431637.1:n.*25_*26delinsTG
ENST00000487921.5:n.509_510delinsTG
ENST00000583539.5:c.597_598delinsTG ENSP00000463121.1:p.Thr200Ala
ENST00000584617.5:c.319_320delinsTG
ENST00000697677.1:n.1678_1679delinsTG
ENST00000697678.1:n.499_500delinsTG
ENST00000697679.1:n.1671_1672delinsTG
ENST00000697680.1:c.*1461_*1462delinsTG ENSP00000513392.1:n.*1461_*1462delinsTG
ENST00000697681.1:c.*1613_*1614delinsTG ENSP00000513393.1:n.*1613_*1614delinsTG
ENST00000697683.1:c.*1461_*1462delinsTG ENSP00000513395.1:n.*1461_*1462delinsTG
ENST00000697684.1:n.657_658delinsTG
ENST00000697685.1:c.*1294_*1295delinsTG ENSP00000513396.1:n.*1294_*1295delinsTG
ENST00000697686.1:c.246_247delinsTG ENSP00000513397.1:p.Thr83Ala
ENST00000697687.1:n.476_477delinsTG
ENST00000697688.1:n.643_644delinsTG
ENST00000697689.1:c.*1133_*1134delinsTG ENSP00000513398.1:n.*1133_*1134delinsTG
ENST00000697690.1:c.597_598delinsTG ENSP00000513399.1:p.Thr200Ala
ENST00000697691.1:c.*569_*570delinsTG ENSP00000513400.1:n.*569_*570delinsTG
ENST00000697692.1:c.*609_*610delinsTG ENSP00000513401.1:n.*609_*610delinsTG
ENST00000697694.1:c.246_247delinsTG ENSP00000513402.1:p.Thr83Ala
ENST00000697695.1:n.1204_1205delinsTG
XM_006722001.2:c.597_598delinsTG XP_006722064.1:p.Thr200Ala
XM_006722001.4:c.597_598delinsTG XP_006722064.1:p.Thr200Ala
XM_006722002.2:c.597_598delinsTG XP_006722065.1:p.Thr200Ala
XM_006722002.4:c.597_598delinsTG XP_006722065.1:p.Thr200Ala
XM_006722004.2:c.246_247delinsTG XP_006722067.1:p.Thr83Ala
XM_006722004.3:c.246_247delinsTG XP_006722067.1:p.Thr83Ala
XM_006722005.2:c.246_247delinsTG XP_006722068.1:p.Thr83Ala
XM_006722005.3:c.246_247delinsTG XP_006722068.1:p.Thr83Ala
XM_011525092.1:c.246_247delinsTG XP_011523394.1:p.Thr83Ala
XM_011525092.2:c.246_247delinsTG XP_011523394.1:p.Thr83Ala
XM_011525093.1:c.246_247delinsTG XP_011523395.1:p.Thr83Ala
XM_011525093.2:c.246_247delinsTG XP_011523395.1:p.Thr83Ala
XM_011525094.1:c.246_247delinsTG XP_011523396.1:p.Thr83Ala
XM_011525094.2:c.246_247delinsTG XP_011523396.1:p.Thr83Ala
XM_017024914.1:c.246_247delinsTG XP_016880403.1:p.Thr83Ala
XM_017024915.1:c.246_247delinsTG XP_016880404.1:p.Thr83Ala
XM_017024916.1:c.246_247delinsTG XP_016880405.1:p.Thr83Ala
XM_017024917.1:c.246_247delinsTG XP_016880406.1:p.Thr83Ala
XM_017024918.2:c.246_247delinsTG XP_016880407.1:p.Thr83Ala
XM_017024919.1:c.246_247delinsTG XP_016880408.1:p.Thr83Ala
XR_934513.1:n.670_671delinsTG
XR_934513.3:n.1101_1102delinsTG
XR_934514.1:n.670_671delinsTG
XR_934514.3:n.1101_1102delinsTG