Canonical Allele Identifier: CA3259239708
Community Standard Title: NM_058216.3(RAD51C):c.60_61delinsAG (p.Pro21Ala)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692703_58692704delinsAG , CM000679.2:g.58692703_58692704delinsAG GRCh38
NC_000017.10:g.56770064_56770065delinsAG , CM000679.1:g.56770064_56770065delinsAG GRCh37
NC_000017.9:g.54125063_54125064delinsAG NCBI36
NG_023199.1:g.5102_5103delinsAG , LRG_314:g.5102_5103delinsAG
NG_047169.1:g.4376_4377delinsCT

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.60_61delinsAG MANE Select NP_478123.1:p.Pro21Ala
ENST00000337432.9:c.60_61delinsAG MANE Select ENSP00000336701.4:p.Pro21Ala
NM_002876.3:c.60_61delinsAG NP_002867.1:p.Pro21Ala
NM_002876.4:c.60_61delinsAG NP_002867.1:p.Pro21Ala
NM_058216.2:c.60_61delinsAG NP_478123.1:p.Pro21Ala
NR_103872.1:n.131_132delinsAG
NR_103872.2:n.102_103delinsAG
NR_103873.1:n.113+18_113+19delinsAG
ENST00000337432.8:c.60_61delinsAG ENSP00000336701.4:p.Pro21Ala
ENST00000421782.3:c.60_61delinsAG ENSP00000391450.2:p.Pro21Ala
ENST00000461271.5:c.-207+18_-207+19delinsAG ENSP00000464056.1:n.-207+18_-207+19delinsAG
ENST00000461271.6:c.-207+18_-207+19delinsAG ENSP00000464056.2:n.-207+18_-207+19delinsAG
ENST00000475762.5:c.60_61delinsAG ENSP00000432421.1:p.Pro21Ala
ENST00000476741.2:n.102_103delinsAG
ENST00000482007.5:c.60_61delinsAG ENSP00000433332.1:p.Pro21Ala
ENST00000486827.1:c.60_61delinsAG ENSP00000436761.1:p.Pro21Ala
ENST00000487525.5:c.60_61delinsAG ENSP00000431637.1:p.Pro21Ala
ENST00000487921.5:n.57+71_57+72delinsAG
ENST00000583539.5:c.60_61delinsAG ENSP00000463121.1:p.Pro21Ala
ENST00000584617.5:c.41_42delinsAG
ENST00000697675.1:n.131_132delinsAG
ENST00000697676.1:n.120_121delinsAG
ENST00000697677.1:n.118_119delinsAG
ENST00000697678.1:n.47+71_47+72delinsAG
ENST00000697679.1:n.111_112delinsAG
ENST00000697680.1:c.60_61delinsAG ENSP00000513392.1:p.Pro21Ala
ENST00000697681.1:c.60_61delinsAG ENSP00000513393.1:p.Pro21Ala
ENST00000697683.1:c.60_61delinsAG ENSP00000513395.1:p.Pro21Ala
ENST00000697684.1:n.120_121delinsAG
ENST00000697685.1:c.60_61delinsAG ENSP00000513396.1:p.Pro21Ala
ENST00000697686.1:c.-207+71_-207+72delinsAG ENSP00000513397.1:n.-207+71_-207+72delinsAG
ENST00000697687.1:n.106_107delinsAG
ENST00000697688.1:n.106_107delinsAG
ENST00000697689.1:c.60_61delinsAG ENSP00000513398.1:p.Pro21Ala
ENST00000697690.1:c.60_61delinsAG ENSP00000513399.1:p.Pro21Ala
ENST00000697691.1:c.42+18_42+19delinsAG ENSP00000513400.1:n.42+18_42+19delinsAG
ENST00000697692.1:c.60_61delinsAG ENSP00000513401.1:p.Pro21Ala
XM_006722001.2:c.60_61delinsAG XP_006722064.1:p.Pro21Ala
XM_006722001.4:c.60_61delinsAG XP_006722064.1:p.Pro21Ala
XM_006722002.2:c.60_61delinsAG XP_006722065.1:p.Pro21Ala
XM_006722002.4:c.60_61delinsAG XP_006722065.1:p.Pro21Ala
XM_006722004.2:c.-207+18_-207+19delinsAG XP_006722067.1:n.-207+18_-207+19delinsAG
XM_006722004.3:c.-207+18_-207+19delinsAG XP_006722067.1:n.-207+18_-207+19delinsAG
XM_006722005.2:c.-207+71_-207+72delinsAG XP_006722068.1:n.-207+71_-207+72delinsAG
XM_006722005.3:c.-207+71_-207+72delinsAG XP_006722068.1:n.-207+71_-207+72delinsAG
XM_011525092.1:c.-507+18_-507+19delinsAG XP_011523394.1:n.-507+18_-507+19delinsAG
XM_011525092.2:c.-507+18_-507+19delinsAG XP_011523394.1:n.-507+18_-507+19delinsAG
XM_011525093.1:c.-668+18_-668+19delinsAG XP_011523395.1:n.-668+18_-668+19delinsAG
XM_011525093.2:c.-668+18_-668+19delinsAG XP_011523395.1:n.-668+18_-668+19delinsAG
XM_017024914.1:c.-207+18_-207+19delinsAG XP_016880403.1:n.-207+18_-207+19delinsAG
XM_017024916.1:c.-507+18_-507+19delinsAG XP_016880405.1:n.-507+18_-507+19delinsAG
XM_017024917.1:c.-207+71_-207+72delinsAG XP_016880406.1:n.-207+71_-207+72delinsAG
XM_017024918.2:c.-463_-462delinsAG XP_016880407.1:n.-463_-462delinsAG
XM_017024919.1:c.-668+18_-668+19delinsAG XP_016880408.1:n.-668+18_-668+19delinsAG
XR_934513.1:n.133_134delinsAG
XR_934513.3:n.564_565delinsAG
XR_934514.1:n.133_134delinsAG
XR_934514.3:n.564_565delinsAG