Canonical Allele Identifier: CA3057243514
Community Standard Title: NM_058216.3(RAD51C):c.1053_1055delinsAGA (p.Thr352Asp)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734144_58734146delinsAGA , CM000679.2:g.58734144_58734146delinsAGA GRCh38
NC_000017.10:g.56811505_56811507delinsAGA , CM000679.1:g.56811505_56811507delinsAGA GRCh37
NC_000017.9:g.54166504_54166506delinsAGA NCBI36
NG_023199.1:g.46543_46545delinsAGA , LRG_314:g.46543_46545delinsAGA

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1053_1055delinsAGA MANE Select NP_478123.1:p.Thr352Asp
ENST00000337432.9:c.1053_1055delinsAGA MANE Select ENSP00000336701.4:p.Thr352Asp
NM_058216.2:c.1053_1055delinsAGA NP_478123.1:p.Thr352Asp
NR_103872.1:n.957_959delinsAGA
NR_103872.2:n.928_930delinsAGA
ENST00000337432.8:c.1053_1055delinsAGA ENSP00000336701.4:p.Thr352Asp
ENST00000413590.5:c.694_696delinsAGA
ENST00000461271.6:c.*1585_*1587delinsAGA ENSP00000464056.2:n.*1585_*1587delinsAGA
ENST00000461706.1:n.240_242delinsAGA
ENST00000475762.5:c.*1689_*1691delinsAGA ENSP00000432421.1:n.*1689_*1691delinsAGA
ENST00000482007.5:c.*481_*483delinsAGA ENSP00000433332.1:n.*481_*483delinsAGA
ENST00000487525.5:c.*629_*631delinsAGA ENSP00000431637.1:n.*629_*631delinsAGA
ENST00000578151.1:n.266_268delinsAGA
ENST00000581221.5:n.568_570delinsAGA
ENST00000584804.1:c.287_289delinsAGA ENSP00000463658.1:p.Leu96Ter
ENST00000697680.1:c.*2017_*2019delinsAGA ENSP00000513392.1:n.*2017_*2019delinsAGA
ENST00000697681.1:c.*2214_*2216delinsAGA ENSP00000513393.1:n.*2214_*2216delinsAGA
ENST00000697683.1:c.*1989_*1991delinsAGA ENSP00000513395.1:n.*1989_*1991delinsAGA
ENST00000697685.1:c.*1750_*1752delinsAGA ENSP00000513396.1:n.*1750_*1752delinsAGA
ENST00000697686.1:c.824_826delinsAGA ENSP00000513397.1:p.Leu275Ter
ENST00000697689.1:c.*1467_*1469delinsAGA ENSP00000513398.1:n.*1467_*1469delinsAGA
ENST00000697690.1:c.*13_*15delinsAGA ENSP00000513399.1:n.*13_*15delinsAGA
ENST00000697691.1:c.*1025_*1027delinsAGA ENSP00000513400.1:n.*1025_*1027delinsAGA
ENST00000697692.1:c.*1065_*1067delinsAGA ENSP00000513401.1:n.*1065_*1067delinsAGA
ENST00000697694.1:c.702_704delinsAGA ENSP00000513402.1:p.Thr235Asp
ENST00000697695.1:n.1660_1662delinsAGA
XM_006722001.2:c.1056_1058delinsAGA XP_006722064.1:p.Thr353Asp
XM_006722001.4:c.1056_1058delinsAGA XP_006722064.1:p.Thr353Asp
XM_006722002.2:c.992_994delinsAGA XP_006722065.1:p.Leu331Ter
XM_006722002.4:c.992_994delinsAGA XP_006722065.1:p.Leu331Ter
XM_006722004.2:c.705_707delinsAGA XP_006722067.1:p.Thr236Asp
XM_006722004.3:c.705_707delinsAGA XP_006722067.1:p.Thr236Asp
XM_006722005.2:c.705_707delinsAGA XP_006722068.1:p.Thr236Asp
XM_006722005.3:c.705_707delinsAGA XP_006722068.1:p.Thr236Asp
XM_011525092.1:c.705_707delinsAGA XP_011523394.1:p.Thr236Asp
XM_011525092.2:c.705_707delinsAGA XP_011523394.1:p.Thr236Asp
XM_011525093.1:c.705_707delinsAGA XP_011523395.1:p.Thr236Asp
XM_011525093.2:c.705_707delinsAGA XP_011523395.1:p.Thr236Asp
XM_011525094.1:c.705_707delinsAGA XP_011523396.1:p.Thr236Asp
XM_011525094.2:c.705_707delinsAGA XP_011523396.1:p.Thr236Asp
XM_017024914.1:c.702_704delinsAGA XP_016880403.1:p.Thr235Asp
XM_017024915.1:c.702_704delinsAGA XP_016880404.1:p.Thr235Asp
XM_017024916.1:c.702_704delinsAGA XP_016880405.1:p.Thr235Asp
XM_017024917.1:c.702_704delinsAGA XP_016880406.1:p.Thr235Asp
XM_017024918.2:c.702_704delinsAGA XP_016880407.1:p.Thr235Asp
XM_017024919.1:c.641_643delinsAGA XP_016880408.1:p.Leu214Ter
XR_934513.1:n.1271_1273delinsAGA
XR_934513.3:n.1702_1704delinsAGA
XR_934514.1:n.1274_1276delinsAGA
XR_934514.3:n.1705_1707delinsAGA
XR_934886.1:n.149+3925_149+3927delinsTCT
XR_934886.2:n.149+3925_149+3927delinsTCT