Canonical Allele Identifier: CA3261179068
Community Standard Title: NM_058216.3(RAD51C):c.883_885delinsACA (p.Ala295Thr)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58720791_58720793delinsACA , CM000679.2:g.58720791_58720793delinsACA GRCh38
NC_000017.10:g.56798152_56798154delinsACA , CM000679.1:g.56798152_56798154delinsACA GRCh37
NC_000017.9:g.54153151_54153153delinsACA NCBI36
NG_023199.1:g.33190_33192delinsACA , LRG_314:g.33190_33192delinsACA

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.883_885delinsACA MANE Select NP_478123.1:p.Ala295Thr
ENST00000337432.9:c.883_885delinsACA MANE Select ENSP00000336701.4:p.Ala295Thr
NM_058216.2:c.883_885delinsACA NP_478123.1:p.Ala295Thr
NR_103872.1:n.787_789delinsACA
NR_103872.2:n.758_760delinsACA
ENST00000337432.8:c.883_885delinsACA ENSP00000336701.4:p.Ala295Thr
ENST00000413590.5:c.521_523delinsACA
ENST00000461271.6:c.532_534delinsACA ENSP00000464056.2:p.Ala178Thr
ENST00000475762.5:c.*1541-3249_*1541-3247delinsACA ENSP00000432421.1:n.*1541-3249_*1541-3247delinsACA
ENST00000482007.5:c.*311_*313delinsACA ENSP00000433332.1:n.*311_*313delinsACA
ENST00000487525.5:c.*456_*458delinsACA ENSP00000431637.1:n.*456_*458delinsACA
ENST00000578151.1:n.218_220delinsACA
ENST00000581221.5:n.398_400delinsACA
ENST00000583539.5:c.883_885delinsACA ENSP00000463121.1:p.Ala295Thr
ENST00000584617.5:c.605_607delinsACA
ENST00000584804.1:c.178_180delinsACA ENSP00000463658.1:p.Ala60Thr
ENST00000697678.1:n.785_787delinsACA
ENST00000697679.1:n.1957_1959delinsACA
ENST00000697680.1:c.*1847_*1849delinsACA ENSP00000513392.1:n.*1847_*1849delinsACA
ENST00000697681.1:c.*2044_*2046delinsACA ENSP00000513393.1:n.*2044_*2046delinsACA
ENST00000697683.1:c.*1747_*1749delinsACA ENSP00000513395.1:n.*1747_*1749delinsACA
ENST00000697684.1:n.943_945delinsACA
ENST00000697685.1:c.*1580_*1582delinsACA ENSP00000513396.1:n.*1580_*1582delinsACA
ENST00000697686.1:c.532_534delinsACA ENSP00000513397.1:p.Ala178Thr
ENST00000697687.1:n.762_764delinsACA
ENST00000697688.1:n.929_931delinsACA
ENST00000697689.1:c.*1419_*1421delinsACA ENSP00000513398.1:n.*1419_*1421delinsACA
ENST00000697690.1:c.883_885delinsACA ENSP00000513399.1:p.Ala295Thr
ENST00000697691.1:c.*855_*857delinsACA ENSP00000513400.1:n.*855_*857delinsACA
ENST00000697692.1:c.*895_*897delinsACA ENSP00000513401.1:n.*895_*897delinsACA
ENST00000697694.1:c.532_534delinsACA ENSP00000513402.1:p.Ala178Thr
ENST00000697695.1:n.1490_1492delinsACA
XM_006722001.2:c.883_885delinsACA XP_006722064.1:p.Ala295Thr
XM_006722001.4:c.883_885delinsACA XP_006722064.1:p.Ala295Thr
XM_006722002.2:c.883_885delinsACA XP_006722065.1:p.Ala295Thr
XM_006722002.4:c.883_885delinsACA XP_006722065.1:p.Ala295Thr
XM_006722004.2:c.532_534delinsACA XP_006722067.1:p.Ala178Thr
XM_006722004.3:c.532_534delinsACA XP_006722067.1:p.Ala178Thr
XM_006722005.2:c.532_534delinsACA XP_006722068.1:p.Ala178Thr
XM_006722005.3:c.532_534delinsACA XP_006722068.1:p.Ala178Thr
XM_011525092.1:c.532_534delinsACA XP_011523394.1:p.Ala178Thr
XM_011525092.2:c.532_534delinsACA XP_011523394.1:p.Ala178Thr
XM_011525093.1:c.532_534delinsACA XP_011523395.1:p.Ala178Thr
XM_011525093.2:c.532_534delinsACA XP_011523395.1:p.Ala178Thr
XM_011525094.1:c.532_534delinsACA XP_011523396.1:p.Ala178Thr
XM_011525094.2:c.532_534delinsACA XP_011523396.1:p.Ala178Thr
XM_017024914.1:c.532_534delinsACA XP_016880403.1:p.Ala178Thr
XM_017024915.1:c.532_534delinsACA XP_016880404.1:p.Ala178Thr
XM_017024916.1:c.532_534delinsACA XP_016880405.1:p.Ala178Thr
XM_017024917.1:c.532_534delinsACA XP_016880406.1:p.Ala178Thr
XM_017024918.2:c.532_534delinsACA XP_016880407.1:p.Ala178Thr
XM_017024919.1:c.532_534delinsACA XP_016880408.1:p.Ala178Thr
XR_934513.1:n.1101_1103delinsACA
XR_934513.3:n.1532_1534delinsACA
XR_934514.1:n.1101_1103delinsACA
XR_934514.3:n.1532_1534delinsACA