Canonical Allele Identifier: CA3261179088
Community Standard Title: NM_058216.3(RAD51C):c.884_885delinsTG (p.Ala295Val)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58720792_58720793delinsTG , CM000679.2:g.58720792_58720793delinsTG GRCh38
NC_000017.10:g.56798153_56798154delinsTG , CM000679.1:g.56798153_56798154delinsTG GRCh37
NC_000017.9:g.54153152_54153153delinsTG NCBI36
NG_023199.1:g.33191_33192delinsTG , LRG_314:g.33191_33192delinsTG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.884_885delinsTG MANE Select NP_478123.1:p.Ala295Val
ENST00000337432.9:c.884_885delinsTG MANE Select ENSP00000336701.4:p.Ala295Val
NM_058216.2:c.884_885delinsTG NP_478123.1:p.Ala295Val
NR_103872.1:n.788_789delinsTG
NR_103872.2:n.759_760delinsTG
ENST00000337432.8:c.884_885delinsTG ENSP00000336701.4:p.Ala295Val
ENST00000413590.5:c.522_523delinsTG
ENST00000461271.6:c.533_534delinsTG ENSP00000464056.2:p.Ala178Val
ENST00000475762.5:c.*1541-3248_*1541-3247delinsTG ENSP00000432421.1:n.*1541-3248_*1541-3247delinsTG
ENST00000482007.5:c.*312_*313delinsTG ENSP00000433332.1:n.*312_*313delinsTG
ENST00000487525.5:c.*457_*458delinsTG ENSP00000431637.1:n.*457_*458delinsTG
ENST00000578151.1:n.219_220delinsTG
ENST00000581221.5:n.399_400delinsTG
ENST00000583539.5:c.884_885delinsTG ENSP00000463121.1:p.Ala295Val
ENST00000584617.5:c.606_607delinsTG
ENST00000584804.1:c.179_180delinsTG ENSP00000463658.1:p.Ala60Val
ENST00000697678.1:n.786_787delinsTG
ENST00000697679.1:n.1958_1959delinsTG
ENST00000697680.1:c.*1848_*1849delinsTG ENSP00000513392.1:n.*1848_*1849delinsTG
ENST00000697681.1:c.*2045_*2046delinsTG ENSP00000513393.1:n.*2045_*2046delinsTG
ENST00000697683.1:c.*1748_*1749delinsTG ENSP00000513395.1:n.*1748_*1749delinsTG
ENST00000697684.1:n.944_945delinsTG
ENST00000697685.1:c.*1581_*1582delinsTG ENSP00000513396.1:n.*1581_*1582delinsTG
ENST00000697686.1:c.533_534delinsTG ENSP00000513397.1:p.Ala178Val
ENST00000697687.1:n.763_764delinsTG
ENST00000697688.1:n.930_931delinsTG
ENST00000697689.1:c.*1420_*1421delinsTG ENSP00000513398.1:n.*1420_*1421delinsTG
ENST00000697690.1:c.884_885delinsTG ENSP00000513399.1:p.Ala295Val
ENST00000697691.1:c.*856_*857delinsTG ENSP00000513400.1:n.*856_*857delinsTG
ENST00000697692.1:c.*896_*897delinsTG ENSP00000513401.1:n.*896_*897delinsTG
ENST00000697694.1:c.533_534delinsTG ENSP00000513402.1:p.Ala178Val
ENST00000697695.1:n.1491_1492delinsTG
XM_006722001.2:c.884_885delinsTG XP_006722064.1:p.Ala295Val
XM_006722001.4:c.884_885delinsTG XP_006722064.1:p.Ala295Val
XM_006722002.2:c.884_885delinsTG XP_006722065.1:p.Ala295Val
XM_006722002.4:c.884_885delinsTG XP_006722065.1:p.Ala295Val
XM_006722004.2:c.533_534delinsTG XP_006722067.1:p.Ala178Val
XM_006722004.3:c.533_534delinsTG XP_006722067.1:p.Ala178Val
XM_006722005.2:c.533_534delinsTG XP_006722068.1:p.Ala178Val
XM_006722005.3:c.533_534delinsTG XP_006722068.1:p.Ala178Val
XM_011525092.1:c.533_534delinsTG XP_011523394.1:p.Ala178Val
XM_011525092.2:c.533_534delinsTG XP_011523394.1:p.Ala178Val
XM_011525093.1:c.533_534delinsTG XP_011523395.1:p.Ala178Val
XM_011525093.2:c.533_534delinsTG XP_011523395.1:p.Ala178Val
XM_011525094.1:c.533_534delinsTG XP_011523396.1:p.Ala178Val
XM_011525094.2:c.533_534delinsTG XP_011523396.1:p.Ala178Val
XM_017024914.1:c.533_534delinsTG XP_016880403.1:p.Ala178Val
XM_017024915.1:c.533_534delinsTG XP_016880404.1:p.Ala178Val
XM_017024916.1:c.533_534delinsTG XP_016880405.1:p.Ala178Val
XM_017024917.1:c.533_534delinsTG XP_016880406.1:p.Ala178Val
XM_017024918.2:c.533_534delinsTG XP_016880407.1:p.Ala178Val
XM_017024919.1:c.533_534delinsTG XP_016880408.1:p.Ala178Val
XR_934513.1:n.1102_1103delinsTG
XR_934513.3:n.1533_1534delinsTG
XR_934514.1:n.1102_1103delinsTG
XR_934514.3:n.1533_1534delinsTG