Canonical Allele Identifier: CA3057228369
Community Standard Title: NM_058216.3(RAD51C):c.820_821delinsTC (p.Asn274Ser)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709973_58709974delinsTC , CM000679.2:g.58709973_58709974delinsTC GRCh38
NC_000017.10:g.56787334_56787335delinsTC , CM000679.1:g.56787334_56787335delinsTC GRCh37
NC_000017.9:g.54142333_54142334delinsTC NCBI36
NG_023199.1:g.22372_22373delinsTC , LRG_314:g.22372_22373delinsTC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.820_821delinsTC MANE Select NP_478123.1:p.Asn274Ser
ENST00000337432.9:c.820_821delinsTC MANE Select ENSP00000336701.4:p.Asn274Ser
NM_058216.2:c.820_821delinsTC NP_478123.1:p.Asn274Ser
NR_103872.1:n.724_725delinsTC
NR_103872.2:n.695_696delinsTC
ENST00000337432.8:c.820_821delinsTC ENSP00000336701.4:p.Asn274Ser
ENST00000413590.5:c.458_459delinsTC
ENST00000461271.6:c.469_470delinsTC ENSP00000464056.2:p.Asn157Ser
ENST00000475762.5:c.*1523_*1524delinsTC ENSP00000432421.1:n.*1523_*1524delinsTC
ENST00000482007.5:c.*248_*249delinsTC ENSP00000433332.1:n.*248_*249delinsTC
ENST00000487525.5:c.*393_*394delinsTC ENSP00000431637.1:n.*393_*394delinsTC
ENST00000578151.1:n.155_156delinsTC
ENST00000581221.5:n.335_336delinsTC
ENST00000583539.5:c.820_821delinsTC ENSP00000463121.1:p.Asn274Ser
ENST00000584617.5:c.542_543delinsTC
ENST00000584804.1:c.115_116delinsTC ENSP00000463658.1:p.Asn39Ser
ENST00000697678.1:n.722_723delinsTC
ENST00000697679.1:n.1894_1895delinsTC
ENST00000697680.1:c.*1684_*1685delinsTC ENSP00000513392.1:n.*1684_*1685delinsTC
ENST00000697681.1:c.*1981_*1982delinsTC ENSP00000513393.1:n.*1981_*1982delinsTC
ENST00000697683.1:c.*1684_*1685delinsTC ENSP00000513395.1:n.*1684_*1685delinsTC
ENST00000697684.1:n.880_881delinsTC
ENST00000697685.1:c.*1517_*1518delinsTC ENSP00000513396.1:n.*1517_*1518delinsTC
ENST00000697686.1:c.469_470delinsTC ENSP00000513397.1:p.Asn157Ser
ENST00000697687.1:n.699_700delinsTC
ENST00000697688.1:n.866_867delinsTC
ENST00000697689.1:c.*1356_*1357delinsTC ENSP00000513398.1:n.*1356_*1357delinsTC
ENST00000697690.1:c.820_821delinsTC ENSP00000513399.1:p.Asn274Ser
ENST00000697691.1:c.*792_*793delinsTC ENSP00000513400.1:n.*792_*793delinsTC
ENST00000697692.1:c.*832_*833delinsTC ENSP00000513401.1:n.*832_*833delinsTC
ENST00000697694.1:c.469_470delinsTC ENSP00000513402.1:p.Asn157Ser
ENST00000697695.1:n.1427_1428delinsTC
XM_006722001.2:c.820_821delinsTC XP_006722064.1:p.Asn274Ser
XM_006722001.4:c.820_821delinsTC XP_006722064.1:p.Asn274Ser
XM_006722002.2:c.820_821delinsTC XP_006722065.1:p.Asn274Ser
XM_006722002.4:c.820_821delinsTC XP_006722065.1:p.Asn274Ser
XM_006722004.2:c.469_470delinsTC XP_006722067.1:p.Asn157Ser
XM_006722004.3:c.469_470delinsTC XP_006722067.1:p.Asn157Ser
XM_006722005.2:c.469_470delinsTC XP_006722068.1:p.Asn157Ser
XM_006722005.3:c.469_470delinsTC XP_006722068.1:p.Asn157Ser
XM_011525092.1:c.469_470delinsTC XP_011523394.1:p.Asn157Ser
XM_011525092.2:c.469_470delinsTC XP_011523394.1:p.Asn157Ser
XM_011525093.1:c.469_470delinsTC XP_011523395.1:p.Asn157Ser
XM_011525093.2:c.469_470delinsTC XP_011523395.1:p.Asn157Ser
XM_011525094.1:c.469_470delinsTC XP_011523396.1:p.Asn157Ser
XM_011525094.2:c.469_470delinsTC XP_011523396.1:p.Asn157Ser
XM_017024914.1:c.469_470delinsTC XP_016880403.1:p.Asn157Ser
XM_017024915.1:c.469_470delinsTC XP_016880404.1:p.Asn157Ser
XM_017024916.1:c.469_470delinsTC XP_016880405.1:p.Asn157Ser
XM_017024917.1:c.469_470delinsTC XP_016880406.1:p.Asn157Ser
XM_017024918.2:c.469_470delinsTC XP_016880407.1:p.Asn157Ser
XM_017024919.1:c.469_470delinsTC XP_016880408.1:p.Asn157Ser
XR_934513.1:n.1038_1039delinsTC
XR_934513.3:n.1469_1470delinsTC
XR_934514.1:n.1038_1039delinsTC
XR_934514.3:n.1469_1470delinsTC