Canonical Allele Identifier: CA3261178866
Community Standard Title: NM_058216.3(RAD51C):c.719_720delinsCC (p.Ile240Thr)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709872_58709873delinsCC , CM000679.2:g.58709872_58709873delinsCC GRCh38
NC_000017.10:g.56787233_56787234delinsCC , CM000679.1:g.56787233_56787234delinsCC GRCh37
NC_000017.9:g.54142232_54142233delinsCC NCBI36
NG_023199.1:g.22271_22272delinsCC , LRG_314:g.22271_22272delinsCC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.719_720delinsCC MANE Select NP_478123.1:p.Ile240Thr
ENST00000337432.9:c.719_720delinsCC MANE Select ENSP00000336701.4:p.Ile240Thr
NM_058216.2:c.719_720delinsCC NP_478123.1:p.Ile240Thr
NR_103872.1:n.623_624delinsCC
NR_103872.2:n.594_595delinsCC
ENST00000337432.8:c.719_720delinsCC ENSP00000336701.4:p.Ile240Thr
ENST00000413590.5:c.357_358delinsCC
ENST00000425173.5:c.635_636delinsCC ENSP00000407282.1:p.Ile212Thr
ENST00000461271.5:c.368_369delinsCC ENSP00000464056.1:p.Ile123Thr
ENST00000461271.6:c.368_369delinsCC ENSP00000464056.2:p.Ile123Thr
ENST00000475762.5:c.*1422_*1423delinsCC ENSP00000432421.1:n.*1422_*1423delinsCC
ENST00000482007.5:c.*147_*148delinsCC ENSP00000433332.1:n.*147_*148delinsCC
ENST00000487525.5:c.*292_*293delinsCC ENSP00000431637.1:n.*292_*293delinsCC
ENST00000578151.1:n.54_55delinsCC
ENST00000581221.5:n.234_235delinsCC
ENST00000583539.5:c.719_720delinsCC ENSP00000463121.1:p.Ile240Thr
ENST00000584617.5:c.441_442delinsCC
ENST00000584804.1:c.14_15delinsCC ENSP00000463658.1:p.Ile5Thr
ENST00000697678.1:n.621_622delinsCC
ENST00000697679.1:n.1793_1794delinsCC
ENST00000697680.1:c.*1583_*1584delinsCC ENSP00000513392.1:n.*1583_*1584delinsCC
ENST00000697681.1:c.*1880_*1881delinsCC ENSP00000513393.1:n.*1880_*1881delinsCC
ENST00000697683.1:c.*1583_*1584delinsCC ENSP00000513395.1:n.*1583_*1584delinsCC
ENST00000697684.1:n.779_780delinsCC
ENST00000697685.1:c.*1416_*1417delinsCC ENSP00000513396.1:n.*1416_*1417delinsCC
ENST00000697686.1:c.368_369delinsCC ENSP00000513397.1:p.Ile123Thr
ENST00000697687.1:n.598_599delinsCC
ENST00000697688.1:n.765_766delinsCC
ENST00000697689.1:c.*1255_*1256delinsCC ENSP00000513398.1:n.*1255_*1256delinsCC
ENST00000697690.1:c.719_720delinsCC ENSP00000513399.1:p.Ile240Thr
ENST00000697691.1:c.*691_*692delinsCC ENSP00000513400.1:n.*691_*692delinsCC
ENST00000697692.1:c.*731_*732delinsCC ENSP00000513401.1:n.*731_*732delinsCC
ENST00000697694.1:c.368_369delinsCC ENSP00000513402.1:p.Ile123Thr
ENST00000697695.1:n.1326_1327delinsCC
XM_006722001.2:c.719_720delinsCC XP_006722064.1:p.Ile240Thr
XM_006722001.4:c.719_720delinsCC XP_006722064.1:p.Ile240Thr
XM_006722002.2:c.719_720delinsCC XP_006722065.1:p.Ile240Thr
XM_006722002.4:c.719_720delinsCC XP_006722065.1:p.Ile240Thr
XM_006722004.2:c.368_369delinsCC XP_006722067.1:p.Ile123Thr
XM_006722004.3:c.368_369delinsCC XP_006722067.1:p.Ile123Thr
XM_006722005.2:c.368_369delinsCC XP_006722068.1:p.Ile123Thr
XM_006722005.3:c.368_369delinsCC XP_006722068.1:p.Ile123Thr
XM_011525092.1:c.368_369delinsCC XP_011523394.1:p.Ile123Thr
XM_011525092.2:c.368_369delinsCC XP_011523394.1:p.Ile123Thr
XM_011525093.1:c.368_369delinsCC XP_011523395.1:p.Ile123Thr
XM_011525093.2:c.368_369delinsCC XP_011523395.1:p.Ile123Thr
XM_011525094.1:c.368_369delinsCC XP_011523396.1:p.Ile123Thr
XM_011525094.2:c.368_369delinsCC XP_011523396.1:p.Ile123Thr
XM_017024914.1:c.368_369delinsCC XP_016880403.1:p.Ile123Thr
XM_017024915.1:c.368_369delinsCC XP_016880404.1:p.Ile123Thr
XM_017024916.1:c.368_369delinsCC XP_016880405.1:p.Ile123Thr
XM_017024917.1:c.368_369delinsCC XP_016880406.1:p.Ile123Thr
XM_017024918.2:c.368_369delinsCC XP_016880407.1:p.Ile123Thr
XM_017024919.1:c.368_369delinsCC XP_016880408.1:p.Ile123Thr
XR_934513.1:n.937_938delinsCC
XR_934513.3:n.1368_1369delinsCC
XR_934514.1:n.937_938delinsCC
XR_934514.3:n.1368_1369delinsCC