Canonical Allele Identifier: CA3261179209
Community Standard Title: NM_058216.3(RAD51C):c.890_891delinsCC (p.Leu297Pro)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58720798_58720799delinsCC , CM000679.2:g.58720798_58720799delinsCC GRCh38
NC_000017.10:g.56798159_56798160delinsCC , CM000679.1:g.56798159_56798160delinsCC GRCh37
NC_000017.9:g.54153158_54153159delinsCC NCBI36
NG_023199.1:g.33197_33198delinsCC , LRG_314:g.33197_33198delinsCC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.890_891delinsCC MANE Select NP_478123.1:p.Leu297Pro
ENST00000337432.9:c.890_891delinsCC MANE Select ENSP00000336701.4:p.Leu297Pro
NM_058216.2:c.890_891delinsCC NP_478123.1:p.Leu297Pro
NR_103872.1:n.794_795delinsCC
NR_103872.2:n.765_766delinsCC
ENST00000337432.8:c.890_891delinsCC ENSP00000336701.4:p.Leu297Pro
ENST00000413590.5:c.528_529delinsCC
ENST00000461271.6:c.539_540delinsCC ENSP00000464056.2:p.Leu180Pro
ENST00000475762.5:c.*1541-3242_*1541-3241delinsCC ENSP00000432421.1:n.*1541-3242_*1541-3241delinsCC
ENST00000482007.5:c.*318_*319delinsCC ENSP00000433332.1:n.*318_*319delinsCC
ENST00000487525.5:c.*463_*464delinsCC ENSP00000431637.1:n.*463_*464delinsCC
ENST00000578151.1:n.225_226delinsCC
ENST00000581221.5:n.405_406delinsCC
ENST00000583539.5:c.890_891delinsCC ENSP00000463121.1:p.Leu297Pro
ENST00000584617.5:c.612_613delinsCC
ENST00000584804.1:c.185_186delinsCC ENSP00000463658.1:p.Leu62Pro
ENST00000697678.1:n.792_793delinsCC
ENST00000697679.1:n.1964_1965delinsCC
ENST00000697680.1:c.*1854_*1855delinsCC ENSP00000513392.1:n.*1854_*1855delinsCC
ENST00000697681.1:c.*2051_*2052delinsCC ENSP00000513393.1:n.*2051_*2052delinsCC
ENST00000697683.1:c.*1754_*1755delinsCC ENSP00000513395.1:n.*1754_*1755delinsCC
ENST00000697684.1:n.950_951delinsCC
ENST00000697685.1:c.*1587_*1588delinsCC ENSP00000513396.1:n.*1587_*1588delinsCC
ENST00000697686.1:c.539_540delinsCC ENSP00000513397.1:p.Leu180Pro
ENST00000697687.1:n.769_770delinsCC
ENST00000697688.1:n.936_937delinsCC
ENST00000697689.1:c.*1426_*1427delinsCC ENSP00000513398.1:n.*1426_*1427delinsCC
ENST00000697690.1:c.890_891delinsCC ENSP00000513399.1:p.Leu297Pro
ENST00000697691.1:c.*862_*863delinsCC ENSP00000513400.1:n.*862_*863delinsCC
ENST00000697692.1:c.*902_*903delinsCC ENSP00000513401.1:n.*902_*903delinsCC
ENST00000697694.1:c.539_540delinsCC ENSP00000513402.1:p.Leu180Pro
ENST00000697695.1:n.1497_1498delinsCC
XM_006722001.2:c.890_891delinsCC XP_006722064.1:p.Leu297Pro
XM_006722001.4:c.890_891delinsCC XP_006722064.1:p.Leu297Pro
XM_006722002.2:c.890_891delinsCC XP_006722065.1:p.Leu297Pro
XM_006722002.4:c.890_891delinsCC XP_006722065.1:p.Leu297Pro
XM_006722004.2:c.539_540delinsCC XP_006722067.1:p.Leu180Pro
XM_006722004.3:c.539_540delinsCC XP_006722067.1:p.Leu180Pro
XM_006722005.2:c.539_540delinsCC XP_006722068.1:p.Leu180Pro
XM_006722005.3:c.539_540delinsCC XP_006722068.1:p.Leu180Pro
XM_011525092.1:c.539_540delinsCC XP_011523394.1:p.Leu180Pro
XM_011525092.2:c.539_540delinsCC XP_011523394.1:p.Leu180Pro
XM_011525093.1:c.539_540delinsCC XP_011523395.1:p.Leu180Pro
XM_011525093.2:c.539_540delinsCC XP_011523395.1:p.Leu180Pro
XM_011525094.1:c.539_540delinsCC XP_011523396.1:p.Leu180Pro
XM_011525094.2:c.539_540delinsCC XP_011523396.1:p.Leu180Pro
XM_017024914.1:c.539_540delinsCC XP_016880403.1:p.Leu180Pro
XM_017024915.1:c.539_540delinsCC XP_016880404.1:p.Leu180Pro
XM_017024916.1:c.539_540delinsCC XP_016880405.1:p.Leu180Pro
XM_017024917.1:c.539_540delinsCC XP_016880406.1:p.Leu180Pro
XM_017024918.2:c.539_540delinsCC XP_016880407.1:p.Leu180Pro
XM_017024919.1:c.539_540delinsCC XP_016880408.1:p.Leu180Pro
XR_934513.1:n.1108_1109delinsCC
XR_934513.3:n.1539_1540delinsCC
XR_934514.1:n.1108_1109delinsCC
XR_934514.3:n.1539_1540delinsCC