Canonical Allele Identifier: CA3261180063
Community Standard Title: NM_058216.3(RAD51C):c.952_954delinsAAT (p.Asp318Asn)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58724087_58724089delinsAAT , CM000679.2:g.58724087_58724089delinsAAT GRCh38
NC_000017.10:g.56801448_56801450delinsAAT , CM000679.1:g.56801448_56801450delinsAAT GRCh37
NC_000017.9:g.54156447_54156449delinsAAT NCBI36
NG_023199.1:g.36486_36488delinsAAT , LRG_314:g.36486_36488delinsAAT

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.952_954delinsAAT MANE Select NP_478123.1:p.Asp318Asn
ENST00000337432.9:c.952_954delinsAAT MANE Select ENSP00000336701.4:p.Asp318Asn
NM_058216.2:c.952_954delinsAAT NP_478123.1:p.Asp318Asn
NR_103872.1:n.856_858delinsAAT
NR_103872.2:n.827_829delinsAAT
ENST00000337432.8:c.952_954delinsAAT ENSP00000336701.4:p.Asp318Asn
ENST00000413590.5:c.590_592delinsAAT
ENST00000461271.6:c.601_603delinsAAT ENSP00000464056.2:p.Asp201Asn
ENST00000475762.5:c.*1588_*1590delinsAAT ENSP00000432421.1:n.*1588_*1590delinsAAT
ENST00000482007.5:c.*380_*382delinsAAT ENSP00000433332.1:n.*380_*382delinsAAT
ENST00000487525.5:c.*525_*527delinsAAT ENSP00000431637.1:n.*525_*527delinsAAT
ENST00000578151.1:n.239+3275_239+3277delinsAAT
ENST00000581221.5:n.467_469delinsAAT
ENST00000583539.5:c.952_954delinsAAT ENSP00000463121.1:p.Asp318Asn
ENST00000584617.5:c.674_676delinsAAT
ENST00000584804.1:c.199+3275_199+3277delinsAAT ENSP00000463658.1:n.199+3275_199+3277delinsAAT
ENST00000697680.1:c.*1916_*1918delinsAAT ENSP00000513392.1:n.*1916_*1918delinsAAT
ENST00000697681.1:c.*2113_*2115delinsAAT ENSP00000513393.1:n.*2113_*2115delinsAAT
ENST00000697683.1:c.*1816_*1818delinsAAT ENSP00000513395.1:n.*1816_*1818delinsAAT
ENST00000697684.1:n.1012_1014delinsAAT
ENST00000697685.1:c.*1649_*1651delinsAAT ENSP00000513396.1:n.*1649_*1651delinsAAT
ENST00000697686.1:c.601_603delinsAAT ENSP00000513397.1:p.Asp201Asn
ENST00000697687.1:n.831_833delinsAAT
ENST00000697688.1:n.998_1000delinsAAT
ENST00000697689.1:c.*1440+3275_*1440+3277delinsAAT ENSP00000513398.1:n.*1440+3275_*1440+3277delinsAAT
ENST00000697690.1:c.904+3275_904+3277delinsAAT ENSP00000513399.1:n.904+3275_904+3277delinsAAT
ENST00000697691.1:c.*924_*926delinsAAT ENSP00000513400.1:n.*924_*926delinsAAT
ENST00000697692.1:c.*964_*966delinsAAT ENSP00000513401.1:n.*964_*966delinsAAT
ENST00000697694.1:c.601_603delinsAAT ENSP00000513402.1:p.Asp201Asn
ENST00000697695.1:n.1559_1561delinsAAT
XM_006722001.2:c.952_954delinsAAT XP_006722064.1:p.Asp318Asn
XM_006722001.4:c.952_954delinsAAT XP_006722064.1:p.Asp318Asn
XM_006722002.2:c.904+3275_904+3277delinsAAT XP_006722065.1:n.904+3275_904+3277delinsAAT
XM_006722002.4:c.904+3275_904+3277delinsAAT XP_006722065.1:n.904+3275_904+3277delinsAAT
XM_006722004.2:c.601_603delinsAAT XP_006722067.1:p.Asp201Asn
XM_006722004.3:c.601_603delinsAAT XP_006722067.1:p.Asp201Asn
XM_006722005.2:c.601_603delinsAAT XP_006722068.1:p.Asp201Asn
XM_006722005.3:c.601_603delinsAAT XP_006722068.1:p.Asp201Asn
XM_011525092.1:c.601_603delinsAAT XP_011523394.1:p.Asp201Asn
XM_011525092.2:c.601_603delinsAAT XP_011523394.1:p.Asp201Asn
XM_011525093.1:c.601_603delinsAAT XP_011523395.1:p.Asp201Asn
XM_011525093.2:c.601_603delinsAAT XP_011523395.1:p.Asp201Asn
XM_011525094.1:c.601_603delinsAAT XP_011523396.1:p.Asp201Asn
XM_011525094.2:c.601_603delinsAAT XP_011523396.1:p.Asp201Asn
XM_017024914.1:c.601_603delinsAAT XP_016880403.1:p.Asp201Asn
XM_017024915.1:c.601_603delinsAAT XP_016880404.1:p.Asp201Asn
XM_017024916.1:c.601_603delinsAAT XP_016880405.1:p.Asp201Asn
XM_017024917.1:c.601_603delinsAAT XP_016880406.1:p.Asp201Asn
XM_017024918.2:c.601_603delinsAAT XP_016880407.1:p.Asp201Asn
XM_017024919.1:c.553+3275_553+3277delinsAAT XP_016880408.1:n.553+3275_553+3277delinsAAT
XR_934513.1:n.1170_1172delinsAAT
XR_934513.3:n.1601_1603delinsAAT
XR_934514.1:n.1170_1172delinsAAT
XR_934514.3:n.1601_1603delinsAAT