Canonical Allele Identifier: CA3261178842
Community Standard Title: NM_058216.3(RAD51C):c.22_24delinsCTG (p.Phe8Leu)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692665_58692667delinsCTG , CM000679.2:g.58692665_58692667delinsCTG GRCh38
NC_000017.10:g.56770026_56770028delinsCTG , CM000679.1:g.56770026_56770028delinsCTG GRCh37
NC_000017.9:g.54125025_54125027delinsCTG NCBI36
NG_023199.1:g.5064_5066delinsCTG , LRG_314:g.5064_5066delinsCTG
NG_047169.1:g.4413_4415delinsCAG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.22_24delinsCTG MANE Select NP_478123.1:p.Phe8Leu
ENST00000337432.9:c.22_24delinsCTG MANE Select ENSP00000336701.4:p.Phe8Leu
NM_002876.3:c.22_24delinsCTG NP_002867.1:p.Phe8Leu
NM_002876.4:c.22_24delinsCTG NP_002867.1:p.Phe8Leu
NM_058216.2:c.22_24delinsCTG NP_478123.1:p.Phe8Leu
NR_103872.1:n.93_95delinsCTG
NR_103872.2:n.64_66delinsCTG
NR_103873.1:n.93_95delinsCTG
ENST00000337432.8:c.22_24delinsCTG ENSP00000336701.4:p.Phe8Leu
ENST00000421782.3:c.22_24delinsCTG ENSP00000391450.2:p.Phe8Leu
ENST00000461271.5:c.-227_-225delinsCTG ENSP00000464056.1:n.-227_-225delinsCTG
ENST00000461271.6:c.-227_-225delinsCTG ENSP00000464056.2:n.-227_-225delinsCTG
ENST00000475762.5:c.22_24delinsCTG ENSP00000432421.1:p.Phe8Leu
ENST00000476741.2:n.64_66delinsCTG
ENST00000482007.5:c.22_24delinsCTG ENSP00000433332.1:p.Phe8Leu
ENST00000486827.1:c.22_24delinsCTG ENSP00000436761.1:p.Phe8Leu
ENST00000487525.5:c.22_24delinsCTG ENSP00000431637.1:p.Phe8Leu
ENST00000487921.5:n.57+33_57+35delinsCTG
ENST00000583539.5:c.22_24delinsCTG ENSP00000463121.1:p.Phe8Leu
ENST00000584617.5:c.3_5delinsCTG
ENST00000697675.1:n.93_95delinsCTG
ENST00000697676.1:n.82_84delinsCTG
ENST00000697677.1:n.80_82delinsCTG
ENST00000697678.1:n.47+33_47+35delinsCTG
ENST00000697679.1:n.73_75delinsCTG
ENST00000697680.1:c.22_24delinsCTG ENSP00000513392.1:p.Phe8Leu
ENST00000697681.1:c.22_24delinsCTG ENSP00000513393.1:p.Phe8Leu
ENST00000697683.1:c.22_24delinsCTG ENSP00000513395.1:p.Phe8Leu
ENST00000697684.1:n.82_84delinsCTG
ENST00000697685.1:c.22_24delinsCTG ENSP00000513396.1:p.Phe8Leu
ENST00000697686.1:c.-207+33_-207+35delinsCTG ENSP00000513397.1:n.-207+33_-207+35delinsCTG
ENST00000697687.1:n.68_70delinsCTG
ENST00000697688.1:n.68_70delinsCTG
ENST00000697689.1:c.22_24delinsCTG ENSP00000513398.1:p.Phe8Leu
ENST00000697690.1:c.22_24delinsCTG ENSP00000513399.1:p.Phe8Leu
ENST00000697691.1:c.22_24delinsCTG ENSP00000513400.1:p.Phe8Leu
ENST00000697692.1:c.22_24delinsCTG ENSP00000513401.1:p.Phe8Leu
XM_006722001.2:c.22_24delinsCTG XP_006722064.1:p.Phe8Leu
XM_006722001.4:c.22_24delinsCTG XP_006722064.1:p.Phe8Leu
XM_006722002.2:c.22_24delinsCTG XP_006722065.1:p.Phe8Leu
XM_006722002.4:c.22_24delinsCTG XP_006722065.1:p.Phe8Leu
XM_006722004.2:c.-227_-225delinsCTG XP_006722067.1:n.-227_-225delinsCTG
XM_006722004.3:c.-227_-225delinsCTG XP_006722067.1:n.-227_-225delinsCTG
XM_006722005.2:c.-207+33_-207+35delinsCTG XP_006722068.1:n.-207+33_-207+35delinsCTG
XM_006722005.3:c.-207+33_-207+35delinsCTG XP_006722068.1:n.-207+33_-207+35delinsCTG
XM_011525092.1:c.-527_-525delinsCTG XP_011523394.1:n.-527_-525delinsCTG
XM_011525093.1:c.-688_-686delinsCTG XP_011523395.1:n.-688_-686delinsCTG
XM_017024914.1:c.-227_-225delinsCTG XP_016880403.1:n.-227_-225delinsCTG
XM_017024916.1:c.-527_-525delinsCTG XP_016880405.1:n.-527_-525delinsCTG
XM_017024917.1:c.-207+33_-207+35delinsCTG XP_016880406.1:n.-207+33_-207+35delinsCTG
XM_017024918.2:c.-501_-499delinsCTG XP_016880407.1:n.-501_-499delinsCTG
XR_934513.1:n.95_97delinsCTG
XR_934513.3:n.526_528delinsCTG
XR_934514.1:n.95_97delinsCTG
XR_934514.3:n.526_528delinsCTG