Canonical Allele Identifier: CA3261178740
Community Standard Title: NM_058216.3(RAD51C):c.713_714delinsGG (p.Leu238Arg)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709866_58709867delinsGG , CM000679.2:g.58709866_58709867delinsGG GRCh38
NC_000017.10:g.56787227_56787228delinsGG , CM000679.1:g.56787227_56787228delinsGG GRCh37
NC_000017.9:g.54142226_54142227delinsGG NCBI36
NG_023199.1:g.22265_22266delinsGG , LRG_314:g.22265_22266delinsGG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.713_714delinsGG MANE Select NP_478123.1:p.Leu238Arg
ENST00000337432.9:c.713_714delinsGG MANE Select ENSP00000336701.4:p.Leu238Arg
NM_058216.2:c.713_714delinsGG NP_478123.1:p.Leu238Arg
NR_103872.1:n.617_618delinsGG
NR_103872.2:n.588_589delinsGG
ENST00000337432.8:c.713_714delinsGG ENSP00000336701.4:p.Leu238Arg
ENST00000413590.5:c.351_352delinsGG
ENST00000425173.5:c.629_630delinsGG ENSP00000407282.1:p.Leu210Arg
ENST00000461271.5:c.362_363delinsGG ENSP00000464056.1:p.Leu121Arg
ENST00000461271.6:c.362_363delinsGG ENSP00000464056.2:p.Leu121Arg
ENST00000475762.5:c.*1416_*1417delinsGG ENSP00000432421.1:n.*1416_*1417delinsGG
ENST00000482007.5:c.*141_*142delinsGG ENSP00000433332.1:n.*141_*142delinsGG
ENST00000487525.5:c.*286_*287delinsGG ENSP00000431637.1:n.*286_*287delinsGG
ENST00000578151.1:n.48_49delinsGG
ENST00000581221.5:n.228_229delinsGG
ENST00000583539.5:c.713_714delinsGG ENSP00000463121.1:p.Leu238Arg
ENST00000584617.5:c.435_436delinsGG
ENST00000584804.1:c.8_9delinsGG ENSP00000463658.1:p.Leu3Arg
ENST00000697678.1:n.615_616delinsGG
ENST00000697679.1:n.1787_1788delinsGG
ENST00000697680.1:c.*1577_*1578delinsGG ENSP00000513392.1:n.*1577_*1578delinsGG
ENST00000697681.1:c.*1874_*1875delinsGG ENSP00000513393.1:n.*1874_*1875delinsGG
ENST00000697683.1:c.*1577_*1578delinsGG ENSP00000513395.1:n.*1577_*1578delinsGG
ENST00000697684.1:n.773_774delinsGG
ENST00000697685.1:c.*1410_*1411delinsGG ENSP00000513396.1:n.*1410_*1411delinsGG
ENST00000697686.1:c.362_363delinsGG ENSP00000513397.1:p.Leu121Arg
ENST00000697687.1:n.592_593delinsGG
ENST00000697688.1:n.759_760delinsGG
ENST00000697689.1:c.*1249_*1250delinsGG ENSP00000513398.1:n.*1249_*1250delinsGG
ENST00000697690.1:c.713_714delinsGG ENSP00000513399.1:p.Leu238Arg
ENST00000697691.1:c.*685_*686delinsGG ENSP00000513400.1:n.*685_*686delinsGG
ENST00000697692.1:c.*725_*726delinsGG ENSP00000513401.1:n.*725_*726delinsGG
ENST00000697694.1:c.362_363delinsGG ENSP00000513402.1:p.Leu121Arg
ENST00000697695.1:n.1320_1321delinsGG
XM_006722001.2:c.713_714delinsGG XP_006722064.1:p.Leu238Arg
XM_006722001.4:c.713_714delinsGG XP_006722064.1:p.Leu238Arg
XM_006722002.2:c.713_714delinsGG XP_006722065.1:p.Leu238Arg
XM_006722002.4:c.713_714delinsGG XP_006722065.1:p.Leu238Arg
XM_006722004.2:c.362_363delinsGG XP_006722067.1:p.Leu121Arg
XM_006722004.3:c.362_363delinsGG XP_006722067.1:p.Leu121Arg
XM_006722005.2:c.362_363delinsGG XP_006722068.1:p.Leu121Arg
XM_006722005.3:c.362_363delinsGG XP_006722068.1:p.Leu121Arg
XM_011525092.1:c.362_363delinsGG XP_011523394.1:p.Leu121Arg
XM_011525092.2:c.362_363delinsGG XP_011523394.1:p.Leu121Arg
XM_011525093.1:c.362_363delinsGG XP_011523395.1:p.Leu121Arg
XM_011525093.2:c.362_363delinsGG XP_011523395.1:p.Leu121Arg
XM_011525094.1:c.362_363delinsGG XP_011523396.1:p.Leu121Arg
XM_011525094.2:c.362_363delinsGG XP_011523396.1:p.Leu121Arg
XM_017024914.1:c.362_363delinsGG XP_016880403.1:p.Leu121Arg
XM_017024915.1:c.362_363delinsGG XP_016880404.1:p.Leu121Arg
XM_017024916.1:c.362_363delinsGG XP_016880405.1:p.Leu121Arg
XM_017024917.1:c.362_363delinsGG XP_016880406.1:p.Leu121Arg
XM_017024918.2:c.362_363delinsGG XP_016880407.1:p.Leu121Arg
XM_017024919.1:c.362_363delinsGG XP_016880408.1:p.Leu121Arg
XR_934513.1:n.931_932delinsGG
XR_934513.3:n.1362_1363delinsGG
XR_934514.1:n.931_932delinsGG
XR_934514.3:n.1362_1363delinsGG