Canonical Allele Identifier: CA3057242501
Community Standard Title: NM_058216.3(RAD51C):c.627_629delinsAGC (p.Tyr209Ter)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703251_58703253delinsAGC , CM000679.2:g.58703251_58703253delinsAGC GRCh38
NC_000017.10:g.56780612_56780614delinsAGC , CM000679.1:g.56780612_56780614delinsAGC GRCh37
NC_000017.9:g.54135611_54135613delinsAGC NCBI36
NG_023199.1:g.15650_15652delinsAGC , LRG_314:g.15650_15652delinsAGC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.627_629delinsAGC MANE Select NP_478123.1:p.Tyr209Ter
ENST00000337432.9:c.627_629delinsAGC MANE Select ENSP00000336701.4:p.Tyr209Ter
NM_058216.2:c.627_629delinsAGC NP_478123.1:p.Tyr209Ter
NR_103872.1:n.531_533delinsAGC
NR_103872.2:n.502_504delinsAGC
ENST00000337432.8:c.627_629delinsAGC ENSP00000336701.4:p.Tyr209Ter
ENST00000413590.5:c.265_267delinsAGC
ENST00000425173.5:c.423_425delinsAGC ENSP00000407282.1:p.Tyr141Ter
ENST00000461271.5:c.276_278delinsAGC ENSP00000464056.1:p.Tyr92Ter
ENST00000461271.6:c.276_278delinsAGC ENSP00000464056.2:p.Tyr92Ter
ENST00000475762.5:c.*1330_*1332delinsAGC ENSP00000432421.1:n.*1330_*1332delinsAGC
ENST00000482007.5:c.*55_*57delinsAGC ENSP00000433332.1:n.*55_*57delinsAGC
ENST00000487525.5:c.*55_*57delinsAGC ENSP00000431637.1:n.*55_*57delinsAGC
ENST00000487921.5:n.539_541delinsAGC
ENST00000583539.5:c.627_629delinsAGC ENSP00000463121.1:p.Tyr209Ter
ENST00000584617.5:c.349_351delinsAGC
ENST00000697677.1:n.1708_1710delinsAGC
ENST00000697678.1:n.529_531delinsAGC
ENST00000697679.1:n.1701_1703delinsAGC
ENST00000697680.1:c.*1491_*1493delinsAGC ENSP00000513392.1:n.*1491_*1493delinsAGC
ENST00000697681.1:c.*1643_*1645delinsAGC ENSP00000513393.1:n.*1643_*1645delinsAGC
ENST00000697683.1:c.*1491_*1493delinsAGC ENSP00000513395.1:n.*1491_*1493delinsAGC
ENST00000697684.1:n.687_689delinsAGC
ENST00000697685.1:c.*1324_*1326delinsAGC ENSP00000513396.1:n.*1324_*1326delinsAGC
ENST00000697686.1:c.276_278delinsAGC ENSP00000513397.1:p.Tyr92Ter
ENST00000697687.1:n.506_508delinsAGC
ENST00000697688.1:n.673_675delinsAGC
ENST00000697689.1:c.*1163_*1165delinsAGC ENSP00000513398.1:n.*1163_*1165delinsAGC
ENST00000697690.1:c.627_629delinsAGC ENSP00000513399.1:p.Tyr209Ter
ENST00000697691.1:c.*599_*601delinsAGC ENSP00000513400.1:n.*599_*601delinsAGC
ENST00000697692.1:c.*639_*641delinsAGC ENSP00000513401.1:n.*639_*641delinsAGC
ENST00000697694.1:c.276_278delinsAGC ENSP00000513402.1:p.Tyr92Ter
ENST00000697695.1:n.1234_1236delinsAGC
XM_006722001.2:c.627_629delinsAGC XP_006722064.1:p.Tyr209Ter
XM_006722001.4:c.627_629delinsAGC XP_006722064.1:p.Tyr209Ter
XM_006722002.2:c.627_629delinsAGC XP_006722065.1:p.Tyr209Ter
XM_006722002.4:c.627_629delinsAGC XP_006722065.1:p.Tyr209Ter
XM_006722004.2:c.276_278delinsAGC XP_006722067.1:p.Tyr92Ter
XM_006722004.3:c.276_278delinsAGC XP_006722067.1:p.Tyr92Ter
XM_006722005.2:c.276_278delinsAGC XP_006722068.1:p.Tyr92Ter
XM_006722005.3:c.276_278delinsAGC XP_006722068.1:p.Tyr92Ter
XM_011525092.1:c.276_278delinsAGC XP_011523394.1:p.Tyr92Ter
XM_011525092.2:c.276_278delinsAGC XP_011523394.1:p.Tyr92Ter
XM_011525093.1:c.276_278delinsAGC XP_011523395.1:p.Tyr92Ter
XM_011525093.2:c.276_278delinsAGC XP_011523395.1:p.Tyr92Ter
XM_011525094.1:c.276_278delinsAGC XP_011523396.1:p.Tyr92Ter
XM_011525094.2:c.276_278delinsAGC XP_011523396.1:p.Tyr92Ter
XM_017024914.1:c.276_278delinsAGC XP_016880403.1:p.Tyr92Ter
XM_017024915.1:c.276_278delinsAGC XP_016880404.1:p.Tyr92Ter
XM_017024916.1:c.276_278delinsAGC XP_016880405.1:p.Tyr92Ter
XM_017024917.1:c.276_278delinsAGC XP_016880406.1:p.Tyr92Ter
XM_017024918.2:c.276_278delinsAGC XP_016880407.1:p.Tyr92Ter
XM_017024919.1:c.276_278delinsAGC XP_016880408.1:p.Tyr92Ter
XR_934513.1:n.700_702delinsAGC
XR_934513.3:n.1131_1133delinsAGC
XR_934514.1:n.700_702delinsAGC
XR_934514.3:n.1131_1133delinsAGC