Canonical Allele Identifier: CA3261178996
Community Standard Title: NM_058216.3(RAD51C):c.35_36delinsCC (p.Arg12Pro)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692678_58692679delinsCC , CM000679.2:g.58692678_58692679delinsCC GRCh38
NC_000017.10:g.56770039_56770040delinsCC , CM000679.1:g.56770039_56770040delinsCC GRCh37
NC_000017.9:g.54125038_54125039delinsCC NCBI36
NG_023199.1:g.5077_5078delinsCC , LRG_314:g.5077_5078delinsCC
NG_047169.1:g.4401_4402delinsGG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.35_36delinsCC MANE Select NP_478123.1:p.Arg12Pro
ENST00000337432.9:c.35_36delinsCC MANE Select ENSP00000336701.4:p.Arg12Pro
NM_002876.3:c.35_36delinsCC NP_002867.1:p.Arg12Pro
NM_002876.4:c.35_36delinsCC NP_002867.1:p.Arg12Pro
NM_058216.2:c.35_36delinsCC NP_478123.1:p.Arg12Pro
NR_103872.1:n.106_107delinsCC
NR_103872.2:n.77_78delinsCC
NR_103873.1:n.106_107delinsCC
ENST00000337432.8:c.35_36delinsCC ENSP00000336701.4:p.Arg12Pro
ENST00000421782.3:c.35_36delinsCC ENSP00000391450.2:p.Arg12Pro
ENST00000461271.5:c.-214_-213delinsCC ENSP00000464056.1:n.-214_-213delinsCC
ENST00000461271.6:c.-214_-213delinsCC ENSP00000464056.2:n.-214_-213delinsCC
ENST00000475762.5:c.35_36delinsCC ENSP00000432421.1:p.Arg12Pro
ENST00000476741.2:n.77_78delinsCC
ENST00000482007.5:c.35_36delinsCC ENSP00000433332.1:p.Arg12Pro
ENST00000486827.1:c.35_36delinsCC ENSP00000436761.1:p.Arg12Pro
ENST00000487525.5:c.35_36delinsCC ENSP00000431637.1:p.Arg12Pro
ENST00000487921.5:n.57+46_57+47delinsCC
ENST00000583539.5:c.35_36delinsCC ENSP00000463121.1:p.Arg12Pro
ENST00000584617.5:c.16_17delinsCC
ENST00000697675.1:n.106_107delinsCC
ENST00000697676.1:n.95_96delinsCC
ENST00000697677.1:n.93_94delinsCC
ENST00000697678.1:n.47+46_47+47delinsCC
ENST00000697679.1:n.86_87delinsCC
ENST00000697680.1:c.35_36delinsCC ENSP00000513392.1:p.Arg12Pro
ENST00000697681.1:c.35_36delinsCC ENSP00000513393.1:p.Arg12Pro
ENST00000697683.1:c.35_36delinsCC ENSP00000513395.1:p.Arg12Pro
ENST00000697684.1:n.95_96delinsCC
ENST00000697685.1:c.35_36delinsCC ENSP00000513396.1:p.Arg12Pro
ENST00000697686.1:c.-207+46_-207+47delinsCC ENSP00000513397.1:n.-207+46_-207+47delinsCC
ENST00000697687.1:n.81_82delinsCC
ENST00000697688.1:n.81_82delinsCC
ENST00000697689.1:c.35_36delinsCC ENSP00000513398.1:p.Arg12Pro
ENST00000697690.1:c.35_36delinsCC ENSP00000513399.1:p.Arg12Pro
ENST00000697691.1:c.35_36delinsCC ENSP00000513400.1:p.Arg12Pro
ENST00000697692.1:c.35_36delinsCC ENSP00000513401.1:p.Arg12Pro
XM_006722001.2:c.35_36delinsCC XP_006722064.1:p.Arg12Pro
XM_006722001.4:c.35_36delinsCC XP_006722064.1:p.Arg12Pro
XM_006722002.2:c.35_36delinsCC XP_006722065.1:p.Arg12Pro
XM_006722002.4:c.35_36delinsCC XP_006722065.1:p.Arg12Pro
XM_006722004.2:c.-214_-213delinsCC XP_006722067.1:n.-214_-213delinsCC
XM_006722004.3:c.-214_-213delinsCC XP_006722067.1:n.-214_-213delinsCC
XM_006722005.2:c.-207+46_-207+47delinsCC XP_006722068.1:n.-207+46_-207+47delinsCC
XM_006722005.3:c.-207+46_-207+47delinsCC XP_006722068.1:n.-207+46_-207+47delinsCC
XM_011525092.1:c.-514_-513delinsCC XP_011523394.1:n.-514_-513delinsCC
XM_011525092.2:c.-514_-513delinsCC XP_011523394.1:n.-514_-513delinsCC
XM_011525093.1:c.-675_-674delinsCC XP_011523395.1:n.-675_-674delinsCC
XM_011525093.2:c.-675_-674delinsCC XP_011523395.1:n.-675_-674delinsCC
XM_017024914.1:c.-214_-213delinsCC XP_016880403.1:n.-214_-213delinsCC
XM_017024916.1:c.-514_-513delinsCC XP_016880405.1:n.-514_-513delinsCC
XM_017024917.1:c.-207+46_-207+47delinsCC XP_016880406.1:n.-207+46_-207+47delinsCC
XM_017024918.2:c.-488_-487delinsCC XP_016880407.1:n.-488_-487delinsCC
XM_017024919.1:c.-675_-674delinsCC XP_016880408.1:n.-675_-674delinsCC
XR_934513.1:n.108_109delinsCC
XR_934513.3:n.539_540delinsCC
XR_934514.1:n.108_109delinsCC
XR_934514.3:n.539_540delinsCC