Canonical Allele Identifier: CA3261180531
Community Standard Title: NM_058216.3(RAD51C):c.704_705delinsCC (p.Lys235Thr)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703328_58703329delinsCC , CM000679.2:g.58703328_58703329delinsCC GRCh38
NC_000017.10:g.56780689_56780690delinsCC , CM000679.1:g.56780689_56780690delinsCC GRCh37
NC_000017.9:g.54135688_54135689delinsCC NCBI36
NG_023199.1:g.15727_15728delinsCC , LRG_314:g.15727_15728delinsCC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.704_705delinsCC MANE Select NP_478123.1:p.Lys235Thr
ENST00000337432.9:c.704_705delinsCC MANE Select ENSP00000336701.4:p.Lys235Thr
NM_058216.2:c.704_705delinsCC NP_478123.1:p.Lys235Thr
NR_103872.1:n.608_609delinsCC
NR_103872.2:n.579_580delinsCC
ENST00000337432.8:c.704_705delinsCC ENSP00000336701.4:p.Lys235Thr
ENST00000413590.5:c.342_343delinsCC
ENST00000425173.5:c.500_501delinsCC ENSP00000407282.1:p.Lys167Thr
ENST00000461271.5:c.353_354delinsCC ENSP00000464056.1:p.Lys118Thr
ENST00000461271.6:c.353_354delinsCC ENSP00000464056.2:p.Lys118Thr
ENST00000475762.5:c.*1407_*1408delinsCC ENSP00000432421.1:n.*1407_*1408delinsCC
ENST00000482007.5:c.*132_*133delinsCC ENSP00000433332.1:n.*132_*133delinsCC
ENST00000487525.5:c.*132_*133delinsCC ENSP00000431637.1:n.*132_*133delinsCC
ENST00000487921.5:n.616_617delinsCC
ENST00000583539.5:c.704_705delinsCC ENSP00000463121.1:p.Lys235Thr
ENST00000584617.5:c.426_427delinsCC
ENST00000697677.1:n.1785_1786delinsCC
ENST00000697678.1:n.606_607delinsCC
ENST00000697679.1:n.1778_1779delinsCC
ENST00000697680.1:c.*1568_*1569delinsCC ENSP00000513392.1:n.*1568_*1569delinsCC
ENST00000697681.1:c.*1720_*1721delinsCC ENSP00000513393.1:n.*1720_*1721delinsCC
ENST00000697683.1:c.*1568_*1569delinsCC ENSP00000513395.1:n.*1568_*1569delinsCC
ENST00000697684.1:n.764_765delinsCC
ENST00000697685.1:c.*1401_*1402delinsCC ENSP00000513396.1:n.*1401_*1402delinsCC
ENST00000697686.1:c.353_354delinsCC ENSP00000513397.1:p.Lys118Thr
ENST00000697687.1:n.583_584delinsCC
ENST00000697688.1:n.750_751delinsCC
ENST00000697689.1:c.*1240_*1241delinsCC ENSP00000513398.1:n.*1240_*1241delinsCC
ENST00000697690.1:c.704_705delinsCC ENSP00000513399.1:p.Lys235Thr
ENST00000697691.1:c.*676_*677delinsCC ENSP00000513400.1:n.*676_*677delinsCC
ENST00000697692.1:c.*716_*717delinsCC ENSP00000513401.1:n.*716_*717delinsCC
ENST00000697694.1:c.353_354delinsCC ENSP00000513402.1:p.Lys118Thr
ENST00000697695.1:n.1311_1312delinsCC
XM_006722001.2:c.704_705delinsCC XP_006722064.1:p.Lys235Thr
XM_006722001.4:c.704_705delinsCC XP_006722064.1:p.Lys235Thr
XM_006722002.2:c.704_705delinsCC XP_006722065.1:p.Lys235Thr
XM_006722002.4:c.704_705delinsCC XP_006722065.1:p.Lys235Thr
XM_006722004.2:c.353_354delinsCC XP_006722067.1:p.Lys118Thr
XM_006722004.3:c.353_354delinsCC XP_006722067.1:p.Lys118Thr
XM_006722005.2:c.353_354delinsCC XP_006722068.1:p.Lys118Thr
XM_006722005.3:c.353_354delinsCC XP_006722068.1:p.Lys118Thr
XM_011525092.1:c.353_354delinsCC XP_011523394.1:p.Lys118Thr
XM_011525092.2:c.353_354delinsCC XP_011523394.1:p.Lys118Thr
XM_011525093.1:c.353_354delinsCC XP_011523395.1:p.Lys118Thr
XM_011525093.2:c.353_354delinsCC XP_011523395.1:p.Lys118Thr
XM_011525094.1:c.353_354delinsCC XP_011523396.1:p.Lys118Thr
XM_011525094.2:c.353_354delinsCC XP_011523396.1:p.Lys118Thr
XM_017024914.1:c.353_354delinsCC XP_016880403.1:p.Lys118Thr
XM_017024915.1:c.353_354delinsCC XP_016880404.1:p.Lys118Thr
XM_017024916.1:c.353_354delinsCC XP_016880405.1:p.Lys118Thr
XM_017024917.1:c.353_354delinsCC XP_016880406.1:p.Lys118Thr
XM_017024918.2:c.353_354delinsCC XP_016880407.1:p.Lys118Thr
XM_017024919.1:c.353_354delinsCC XP_016880408.1:p.Lys118Thr
XR_934513.1:n.777_778delinsCC
XR_934513.3:n.1208_1209delinsCC
XR_934514.1:n.777_778delinsCC
XR_934514.3:n.1208_1209delinsCC