Canonical Allele Identifier: CA3261178877
Community Standard Title: NM_058216.3(RAD51C):c.26_27delinsTG (p.Glu9Val)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692669_58692670delinsTG , CM000679.2:g.58692669_58692670delinsTG GRCh38
NC_000017.10:g.56770030_56770031delinsTG , CM000679.1:g.56770030_56770031delinsTG GRCh37
NC_000017.9:g.54125029_54125030delinsTG NCBI36
NG_023199.1:g.5068_5069delinsTG , LRG_314:g.5068_5069delinsTG
NG_047169.1:g.4410_4411delinsCA

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.26_27delinsTG MANE Select NP_478123.1:p.Glu9Val
ENST00000337432.9:c.26_27delinsTG MANE Select ENSP00000336701.4:p.Glu9Val
NM_002876.3:c.26_27delinsTG NP_002867.1:p.Glu9Val
NM_002876.4:c.26_27delinsTG NP_002867.1:p.Glu9Val
NM_058216.2:c.26_27delinsTG NP_478123.1:p.Glu9Val
NR_103872.1:n.97_98delinsTG
NR_103872.2:n.68_69delinsTG
NR_103873.1:n.97_98delinsTG
ENST00000337432.8:c.26_27delinsTG ENSP00000336701.4:p.Glu9Val
ENST00000421782.3:c.26_27delinsTG ENSP00000391450.2:p.Glu9Val
ENST00000461271.5:c.-223_-222delinsTG ENSP00000464056.1:n.-223_-222delinsTG
ENST00000461271.6:c.-223_-222delinsTG ENSP00000464056.2:n.-223_-222delinsTG
ENST00000475762.5:c.26_27delinsTG ENSP00000432421.1:p.Glu9Val
ENST00000476741.2:n.68_69delinsTG
ENST00000482007.5:c.26_27delinsTG ENSP00000433332.1:p.Glu9Val
ENST00000486827.1:c.26_27delinsTG ENSP00000436761.1:p.Glu9Val
ENST00000487525.5:c.26_27delinsTG ENSP00000431637.1:p.Glu9Val
ENST00000487921.5:n.57+37_57+38delinsTG
ENST00000583539.5:c.26_27delinsTG ENSP00000463121.1:p.Glu9Val
ENST00000584617.5:c.7_8delinsTG
ENST00000697675.1:n.97_98delinsTG
ENST00000697676.1:n.86_87delinsTG
ENST00000697677.1:n.84_85delinsTG
ENST00000697678.1:n.47+37_47+38delinsTG
ENST00000697679.1:n.77_78delinsTG
ENST00000697680.1:c.26_27delinsTG ENSP00000513392.1:p.Glu9Val
ENST00000697681.1:c.26_27delinsTG ENSP00000513393.1:p.Glu9Val
ENST00000697683.1:c.26_27delinsTG ENSP00000513395.1:p.Glu9Val
ENST00000697684.1:n.86_87delinsTG
ENST00000697685.1:c.26_27delinsTG ENSP00000513396.1:p.Glu9Val
ENST00000697686.1:c.-207+37_-207+38delinsTG ENSP00000513397.1:n.-207+37_-207+38delinsTG
ENST00000697687.1:n.72_73delinsTG
ENST00000697688.1:n.72_73delinsTG
ENST00000697689.1:c.26_27delinsTG ENSP00000513398.1:p.Glu9Val
ENST00000697690.1:c.26_27delinsTG ENSP00000513399.1:p.Glu9Val
ENST00000697691.1:c.26_27delinsTG ENSP00000513400.1:p.Glu9Val
ENST00000697692.1:c.26_27delinsTG ENSP00000513401.1:p.Glu9Val
XM_006722001.2:c.26_27delinsTG XP_006722064.1:p.Glu9Val
XM_006722001.4:c.26_27delinsTG XP_006722064.1:p.Glu9Val
XM_006722002.2:c.26_27delinsTG XP_006722065.1:p.Glu9Val
XM_006722002.4:c.26_27delinsTG XP_006722065.1:p.Glu9Val
XM_006722004.2:c.-223_-222delinsTG XP_006722067.1:n.-223_-222delinsTG
XM_006722004.3:c.-223_-222delinsTG XP_006722067.1:n.-223_-222delinsTG
XM_006722005.2:c.-207+37_-207+38delinsTG XP_006722068.1:n.-207+37_-207+38delinsTG
XM_006722005.3:c.-207+37_-207+38delinsTG XP_006722068.1:n.-207+37_-207+38delinsTG
XM_011525092.1:c.-523_-522delinsTG XP_011523394.1:n.-523_-522delinsTG
XM_011525093.1:c.-684_-683delinsTG XP_011523395.1:n.-684_-683delinsTG
XM_017024914.1:c.-223_-222delinsTG XP_016880403.1:n.-223_-222delinsTG
XM_017024916.1:c.-523_-522delinsTG XP_016880405.1:n.-523_-522delinsTG
XM_017024917.1:c.-207+37_-207+38delinsTG XP_016880406.1:n.-207+37_-207+38delinsTG
XM_017024918.2:c.-497_-496delinsTG XP_016880407.1:n.-497_-496delinsTG
XR_934513.1:n.99_100delinsTG
XR_934513.3:n.530_531delinsTG
XR_934514.1:n.99_100delinsTG
XR_934514.3:n.530_531delinsTG