Canonical Allele Identifier: CA3261178735
Community Standard Title: NM_058216.3(RAD51C):c.16_18delinsCTG (p.Phe6Leu)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692659_58692661delinsCTG , CM000679.2:g.58692659_58692661delinsCTG GRCh38
NC_000017.10:g.56770020_56770022delinsCTG , CM000679.1:g.56770020_56770022delinsCTG GRCh37
NC_000017.9:g.54125019_54125021delinsCTG NCBI36
NG_023199.1:g.5058_5060delinsCTG , LRG_314:g.5058_5060delinsCTG
NG_047169.1:g.4419_4421delinsCAG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.16_18delinsCTG MANE Select NP_478123.1:p.Phe6Leu
ENST00000337432.9:c.16_18delinsCTG MANE Select ENSP00000336701.4:p.Phe6Leu
NM_002876.3:c.16_18delinsCTG NP_002867.1:p.Phe6Leu
NM_002876.4:c.16_18delinsCTG NP_002867.1:p.Phe6Leu
NM_058216.2:c.16_18delinsCTG NP_478123.1:p.Phe6Leu
NR_103872.1:n.87_89delinsCTG
NR_103872.2:n.58_60delinsCTG
NR_103873.1:n.87_89delinsCTG
ENST00000337432.8:c.16_18delinsCTG ENSP00000336701.4:p.Phe6Leu
ENST00000421782.3:c.16_18delinsCTG ENSP00000391450.2:p.Phe6Leu
ENST00000461271.5:c.-233_-231delinsCTG ENSP00000464056.1:n.-233_-231delinsCTG
ENST00000461271.6:c.-233_-231delinsCTG ENSP00000464056.2:n.-233_-231delinsCTG
ENST00000475762.5:c.16_18delinsCTG ENSP00000432421.1:p.Phe6Leu
ENST00000476741.2:n.58_60delinsCTG
ENST00000482007.5:c.16_18delinsCTG ENSP00000433332.1:p.Phe6Leu
ENST00000486827.1:c.16_18delinsCTG ENSP00000436761.1:p.Phe6Leu
ENST00000487525.5:c.16_18delinsCTG ENSP00000431637.1:p.Phe6Leu
ENST00000487921.5:n.57+27_57+29delinsCTG
ENST00000583539.5:c.16_18delinsCTG ENSP00000463121.1:p.Phe6Leu
ENST00000697675.1:n.87_89delinsCTG
ENST00000697676.1:n.76_78delinsCTG
ENST00000697677.1:n.74_76delinsCTG
ENST00000697678.1:n.47+27_47+29delinsCTG
ENST00000697679.1:n.67_69delinsCTG
ENST00000697680.1:c.16_18delinsCTG ENSP00000513392.1:p.Phe6Leu
ENST00000697681.1:c.16_18delinsCTG ENSP00000513393.1:p.Phe6Leu
ENST00000697683.1:c.16_18delinsCTG ENSP00000513395.1:p.Phe6Leu
ENST00000697684.1:n.76_78delinsCTG
ENST00000697685.1:c.16_18delinsCTG ENSP00000513396.1:p.Phe6Leu
ENST00000697686.1:c.-207+27_-207+29delinsCTG ENSP00000513397.1:n.-207+27_-207+29delinsCTG
ENST00000697687.1:n.62_64delinsCTG
ENST00000697688.1:n.62_64delinsCTG
ENST00000697689.1:c.16_18delinsCTG ENSP00000513398.1:p.Phe6Leu
ENST00000697690.1:c.16_18delinsCTG ENSP00000513399.1:p.Phe6Leu
ENST00000697691.1:c.16_18delinsCTG ENSP00000513400.1:p.Phe6Leu
ENST00000697692.1:c.16_18delinsCTG ENSP00000513401.1:p.Phe6Leu
XM_006722001.2:c.16_18delinsCTG XP_006722064.1:p.Phe6Leu
XM_006722001.4:c.16_18delinsCTG XP_006722064.1:p.Phe6Leu
XM_006722002.2:c.16_18delinsCTG XP_006722065.1:p.Phe6Leu
XM_006722002.4:c.16_18delinsCTG XP_006722065.1:p.Phe6Leu
XM_006722004.2:c.-233_-231delinsCTG XP_006722067.1:n.-233_-231delinsCTG
XM_006722004.3:c.-233_-231delinsCTG XP_006722067.1:n.-233_-231delinsCTG
XM_006722005.2:c.-207+27_-207+29delinsCTG XP_006722068.1:n.-207+27_-207+29delinsCTG
XM_006722005.3:c.-207+27_-207+29delinsCTG XP_006722068.1:n.-207+27_-207+29delinsCTG
XM_011525092.1:c.-533_-531delinsCTG XP_011523394.1:n.-533_-531delinsCTG
XM_011525093.1:c.-694_-692delinsCTG XP_011523395.1:n.-694_-692delinsCTG
XM_017024914.1:c.-233_-231delinsCTG XP_016880403.1:n.-233_-231delinsCTG
XM_017024916.1:c.-533_-531delinsCTG XP_016880405.1:n.-533_-531delinsCTG
XM_017024917.1:c.-207+27_-207+29delinsCTG XP_016880406.1:n.-207+27_-207+29delinsCTG
XM_017024918.2:c.-507_-505delinsCTG XP_016880407.1:n.-507_-505delinsCTG
XR_934513.1:n.89_91delinsCTG
XR_934513.3:n.520_522delinsCTG
XR_934514.1:n.89_91delinsCTG
XR_934514.3:n.520_522delinsCTG