Canonical Allele Identifier: CA3261180203
Community Standard Title: NM_058216.3(RAD51C):c.962_963delinsGG (p.Gln321Arg)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58724097_58724098delinsGG , CM000679.2:g.58724097_58724098delinsGG GRCh38
NC_000017.10:g.56801458_56801459delinsGG , CM000679.1:g.56801458_56801459delinsGG GRCh37
NC_000017.9:g.54156457_54156458delinsGG NCBI36
NG_023199.1:g.36496_36497delinsGG , LRG_314:g.36496_36497delinsGG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.962_963delinsGG MANE Select NP_478123.1:p.Gln321Arg
ENST00000337432.9:c.962_963delinsGG MANE Select ENSP00000336701.4:p.Gln321Arg
NM_058216.2:c.962_963delinsGG NP_478123.1:p.Gln321Arg
NR_103872.1:n.866_867delinsGG
NR_103872.2:n.837_838delinsGG
ENST00000337432.8:c.962_963delinsGG ENSP00000336701.4:p.Gln321Arg
ENST00000413590.5:c.600_601delinsGG
ENST00000461271.6:c.611_612delinsGG ENSP00000464056.2:p.Gln204Arg
ENST00000475762.5:c.*1598_*1599delinsGG ENSP00000432421.1:n.*1598_*1599delinsGG
ENST00000482007.5:c.*390_*391delinsGG ENSP00000433332.1:n.*390_*391delinsGG
ENST00000487525.5:c.*535_*536delinsGG ENSP00000431637.1:n.*535_*536delinsGG
ENST00000578151.1:n.239+3285_239+3286delinsGG
ENST00000581221.5:n.477_478delinsGG
ENST00000583539.5:c.962_963delinsGG ENSP00000463121.1:p.Gln321Arg
ENST00000584617.5:c.684_685delinsGG
ENST00000584804.1:c.199+3285_199+3286delinsGG ENSP00000463658.1:n.199+3285_199+3286delinsGG
ENST00000697680.1:c.*1926_*1927delinsGG ENSP00000513392.1:n.*1926_*1927delinsGG
ENST00000697681.1:c.*2123_*2124delinsGG ENSP00000513393.1:n.*2123_*2124delinsGG
ENST00000697683.1:c.*1826_*1827delinsGG ENSP00000513395.1:n.*1826_*1827delinsGG
ENST00000697684.1:n.1022_1023delinsGG
ENST00000697685.1:c.*1659_*1660delinsGG ENSP00000513396.1:n.*1659_*1660delinsGG
ENST00000697686.1:c.611_612delinsGG ENSP00000513397.1:p.Gln204Arg
ENST00000697687.1:n.841_842delinsGG
ENST00000697688.1:n.1008_1009delinsGG
ENST00000697689.1:c.*1440+3285_*1440+3286delinsGG ENSP00000513398.1:n.*1440+3285_*1440+3286delinsGG
ENST00000697690.1:c.904+3285_904+3286delinsGG ENSP00000513399.1:n.904+3285_904+3286delinsGG
ENST00000697691.1:c.*934_*935delinsGG ENSP00000513400.1:n.*934_*935delinsGG
ENST00000697692.1:c.*974_*975delinsGG ENSP00000513401.1:n.*974_*975delinsGG
ENST00000697694.1:c.611_612delinsGG ENSP00000513402.1:p.Gln204Arg
ENST00000697695.1:n.1569_1570delinsGG
XM_006722001.2:c.962_963delinsGG XP_006722064.1:p.Gln321Arg
XM_006722001.4:c.962_963delinsGG XP_006722064.1:p.Gln321Arg
XM_006722002.2:c.904+3285_904+3286delinsGG XP_006722065.1:n.904+3285_904+3286delinsGG
XM_006722002.4:c.904+3285_904+3286delinsGG XP_006722065.1:n.904+3285_904+3286delinsGG
XM_006722004.2:c.611_612delinsGG XP_006722067.1:p.Gln204Arg
XM_006722004.3:c.611_612delinsGG XP_006722067.1:p.Gln204Arg
XM_006722005.2:c.611_612delinsGG XP_006722068.1:p.Gln204Arg
XM_006722005.3:c.611_612delinsGG XP_006722068.1:p.Gln204Arg
XM_011525092.1:c.611_612delinsGG XP_011523394.1:p.Gln204Arg
XM_011525092.2:c.611_612delinsGG XP_011523394.1:p.Gln204Arg
XM_011525093.1:c.611_612delinsGG XP_011523395.1:p.Gln204Arg
XM_011525093.2:c.611_612delinsGG XP_011523395.1:p.Gln204Arg
XM_011525094.1:c.611_612delinsGG XP_011523396.1:p.Gln204Arg
XM_011525094.2:c.611_612delinsGG XP_011523396.1:p.Gln204Arg
XM_017024914.1:c.611_612delinsGG XP_016880403.1:p.Gln204Arg
XM_017024915.1:c.611_612delinsGG XP_016880404.1:p.Gln204Arg
XM_017024916.1:c.611_612delinsGG XP_016880405.1:p.Gln204Arg
XM_017024917.1:c.611_612delinsGG XP_016880406.1:p.Gln204Arg
XM_017024918.2:c.611_612delinsGG XP_016880407.1:p.Gln204Arg
XM_017024919.1:c.553+3285_553+3286delinsGG XP_016880408.1:n.553+3285_553+3286delinsGG
XR_934513.1:n.1180_1181delinsGG
XR_934513.3:n.1611_1612delinsGG
XR_934514.1:n.1180_1181delinsGG
XR_934514.3:n.1611_1612delinsGG