Canonical Allele Identifier: CA3261179226
Community Standard Title: NM_058216.3(RAD51C):c.49_50delinsAG (p.Phe17Ser)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692692_58692693delinsAG , CM000679.2:g.58692692_58692693delinsAG GRCh38
NC_000017.10:g.56770053_56770054delinsAG , CM000679.1:g.56770053_56770054delinsAG GRCh37
NC_000017.9:g.54125052_54125053delinsAG NCBI36
NG_023199.1:g.5091_5092delinsAG , LRG_314:g.5091_5092delinsAG
NG_047169.1:g.4387_4388delinsCT

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.49_50delinsAG MANE Select NP_478123.1:p.Phe17Ser
ENST00000337432.9:c.49_50delinsAG MANE Select ENSP00000336701.4:p.Phe17Ser
NM_002876.3:c.49_50delinsAG NP_002867.1:p.Phe17Ser
NM_002876.4:c.49_50delinsAG NP_002867.1:p.Phe17Ser
NM_058216.2:c.49_50delinsAG NP_478123.1:p.Phe17Ser
NR_103872.1:n.120_121delinsAG
NR_103872.2:n.91_92delinsAG
NR_103873.1:n.113+7_113+8delinsAG
ENST00000337432.8:c.49_50delinsAG ENSP00000336701.4:p.Phe17Ser
ENST00000421782.3:c.49_50delinsAG ENSP00000391450.2:p.Phe17Ser
ENST00000461271.5:c.-207+7_-207+8delinsAG ENSP00000464056.1:n.-207+7_-207+8delinsAG
ENST00000461271.6:c.-207+7_-207+8delinsAG ENSP00000464056.2:n.-207+7_-207+8delinsAG
ENST00000475762.5:c.49_50delinsAG ENSP00000432421.1:p.Phe17Ser
ENST00000476741.2:n.91_92delinsAG
ENST00000482007.5:c.49_50delinsAG ENSP00000433332.1:p.Phe17Ser
ENST00000486827.1:c.49_50delinsAG ENSP00000436761.1:p.Phe17Ser
ENST00000487525.5:c.49_50delinsAG ENSP00000431637.1:p.Phe17Ser
ENST00000487921.5:n.57+60_57+61delinsAG
ENST00000583539.5:c.49_50delinsAG ENSP00000463121.1:p.Phe17Ser
ENST00000584617.5:c.30_31delinsAG
ENST00000697675.1:n.120_121delinsAG
ENST00000697676.1:n.109_110delinsAG
ENST00000697677.1:n.107_108delinsAG
ENST00000697678.1:n.47+60_47+61delinsAG
ENST00000697679.1:n.100_101delinsAG
ENST00000697680.1:c.49_50delinsAG ENSP00000513392.1:p.Phe17Ser
ENST00000697681.1:c.49_50delinsAG ENSP00000513393.1:p.Phe17Ser
ENST00000697683.1:c.49_50delinsAG ENSP00000513395.1:p.Phe17Ser
ENST00000697684.1:n.109_110delinsAG
ENST00000697685.1:c.49_50delinsAG ENSP00000513396.1:p.Phe17Ser
ENST00000697686.1:c.-207+60_-207+61delinsAG ENSP00000513397.1:n.-207+60_-207+61delinsAG
ENST00000697687.1:n.95_96delinsAG
ENST00000697688.1:n.95_96delinsAG
ENST00000697689.1:c.49_50delinsAG ENSP00000513398.1:p.Phe17Ser
ENST00000697690.1:c.49_50delinsAG ENSP00000513399.1:p.Phe17Ser
ENST00000697691.1:c.42+7_42+8delinsAG ENSP00000513400.1:n.42+7_42+8delinsAG
ENST00000697692.1:c.49_50delinsAG ENSP00000513401.1:p.Phe17Ser
XM_006722001.2:c.49_50delinsAG XP_006722064.1:p.Phe17Ser
XM_006722001.4:c.49_50delinsAG XP_006722064.1:p.Phe17Ser
XM_006722002.2:c.49_50delinsAG XP_006722065.1:p.Phe17Ser
XM_006722002.4:c.49_50delinsAG XP_006722065.1:p.Phe17Ser
XM_006722004.2:c.-207+7_-207+8delinsAG XP_006722067.1:n.-207+7_-207+8delinsAG
XM_006722004.3:c.-207+7_-207+8delinsAG XP_006722067.1:n.-207+7_-207+8delinsAG
XM_006722005.2:c.-207+60_-207+61delinsAG XP_006722068.1:n.-207+60_-207+61delinsAG
XM_006722005.3:c.-207+60_-207+61delinsAG XP_006722068.1:n.-207+60_-207+61delinsAG
XM_011525092.1:c.-507+7_-507+8delinsAG XP_011523394.1:n.-507+7_-507+8delinsAG
XM_011525092.2:c.-507+7_-507+8delinsAG XP_011523394.1:n.-507+7_-507+8delinsAG
XM_011525093.1:c.-668+7_-668+8delinsAG XP_011523395.1:n.-668+7_-668+8delinsAG
XM_011525093.2:c.-668+7_-668+8delinsAG XP_011523395.1:n.-668+7_-668+8delinsAG
XM_017024914.1:c.-207+7_-207+8delinsAG XP_016880403.1:n.-207+7_-207+8delinsAG
XM_017024916.1:c.-507+7_-507+8delinsAG XP_016880405.1:n.-507+7_-507+8delinsAG
XM_017024917.1:c.-207+60_-207+61delinsAG XP_016880406.1:n.-207+60_-207+61delinsAG
XM_017024918.2:c.-474_-473delinsAG XP_016880407.1:n.-474_-473delinsAG
XM_017024919.1:c.-668+7_-668+8delinsAG XP_016880408.1:n.-668+7_-668+8delinsAG
XR_934513.1:n.122_123delinsAG
XR_934513.3:n.553_554delinsAG
XR_934514.1:n.122_123delinsAG
XR_934514.3:n.553_554delinsAG