Canonical Allele Identifier: CA3261180064
Community Standard Title: NM_058216.3(RAD51C):c.377_378delinsTG (p.Ala126Val)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58695162_58695163delinsTG , CM000679.2:g.58695162_58695163delinsTG GRCh38
NC_000017.10:g.56772523_56772524delinsTG , CM000679.1:g.56772523_56772524delinsTG GRCh37
NC_000017.9:g.54127522_54127523delinsTG NCBI36
NG_023199.1:g.7561_7562delinsTG , LRG_314:g.7561_7562delinsTG
NG_047169.1:g.1917_1918delinsCA

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.377_378delinsTG MANE Select NP_478123.1:p.Ala126Val
ENST00000337432.9:c.377_378delinsTG MANE Select ENSP00000336701.4:p.Ala126Val
NM_002876.3:c.377_378delinsTG NP_002867.1:p.Ala126Val
NM_002876.4:c.377_378delinsTG NP_002867.1:p.Ala126Val
NM_058216.2:c.377_378delinsTG NP_478123.1:p.Ala126Val
NR_103872.1:n.448_449delinsTG
NR_103872.2:n.419_420delinsTG
NR_103873.1:n.345_346delinsTG
ENST00000337432.8:c.377_378delinsTG ENSP00000336701.4:p.Ala126Val
ENST00000413590.5:c.15_16delinsTG
ENST00000421782.3:c.377_378delinsTG ENSP00000391450.2:p.Ala126Val
ENST00000425173.5:c.173_174delinsTG ENSP00000407282.1:p.Ala58Val
ENST00000461271.5:c.26_27delinsTG ENSP00000464056.1:p.Ala9Val
ENST00000461271.6:c.26_27delinsTG ENSP00000464056.2:p.Ala9Val
ENST00000475762.5:c.*1080_*1081delinsTG ENSP00000432421.1:n.*1080_*1081delinsTG
ENST00000482007.5:c.377_378delinsTG ENSP00000433332.1:p.Ala126Val
ENST00000486827.1:c.*1241_*1242delinsTG ENSP00000436761.1:n.*1241_*1242delinsTG
ENST00000487525.5:c.377_378delinsTG ENSP00000431637.1:p.Ala126Val
ENST00000487921.5:n.289_290delinsTG
ENST00000583539.5:c.377_378delinsTG ENSP00000463121.1:p.Ala126Val
ENST00000584617.5:c.127-1531_127-1530delinsTG
ENST00000622327.4:c.113_114delinsTG ENSP00000482326.1:p.Ala38Val
ENST00000697675.1:n.1471_1472delinsTG
ENST00000697676.1:n.437_438delinsTG
ENST00000697677.1:n.1458_1459delinsTG
ENST00000697678.1:n.279_280delinsTG
ENST00000697679.1:n.1451_1452delinsTG
ENST00000697680.1:c.*1241_*1242delinsTG ENSP00000513392.1:n.*1241_*1242delinsTG
ENST00000697681.1:c.*1241_*1242delinsTG ENSP00000513393.1:n.*1241_*1242delinsTG
ENST00000697683.1:c.*1241_*1242delinsTG ENSP00000513395.1:n.*1241_*1242delinsTG
ENST00000697684.1:n.437_438delinsTG
ENST00000697685.1:c.*1241_*1242delinsTG ENSP00000513396.1:n.*1241_*1242delinsTG
ENST00000697686.1:c.26_27delinsTG ENSP00000513397.1:p.Ala9Val
ENST00000697687.1:n.423_424delinsTG
ENST00000697688.1:n.423_424delinsTG
ENST00000697689.1:c.*1080_*1081delinsTG ENSP00000513398.1:n.*1080_*1081delinsTG
ENST00000697690.1:c.377_378delinsTG ENSP00000513399.1:p.Ala126Val
ENST00000697691.1:c.*349_*350delinsTG ENSP00000513400.1:n.*349_*350delinsTG
ENST00000697692.1:c.*389_*390delinsTG ENSP00000513401.1:n.*389_*390delinsTG
ENST00000697693.1:n.1152_1153delinsTG
ENST00000697694.1:c.26_27delinsTG ENSP00000513402.1:p.Ala9Val
ENST00000697695.1:n.984_985delinsTG
XM_006722001.2:c.377_378delinsTG XP_006722064.1:p.Ala126Val
XM_006722001.4:c.377_378delinsTG XP_006722064.1:p.Ala126Val
XM_006722002.2:c.377_378delinsTG XP_006722065.1:p.Ala126Val
XM_006722002.4:c.377_378delinsTG XP_006722065.1:p.Ala126Val
XM_006722004.2:c.26_27delinsTG XP_006722067.1:p.Ala9Val
XM_006722004.3:c.26_27delinsTG XP_006722067.1:p.Ala9Val
XM_006722005.2:c.26_27delinsTG XP_006722068.1:p.Ala9Val
XM_006722005.3:c.26_27delinsTG XP_006722068.1:p.Ala9Val
XM_011525092.1:c.26_27delinsTG XP_011523394.1:p.Ala9Val
XM_011525092.2:c.26_27delinsTG XP_011523394.1:p.Ala9Val
XM_011525093.1:c.26_27delinsTG XP_011523395.1:p.Ala9Val
XM_011525093.2:c.26_27delinsTG XP_011523395.1:p.Ala9Val
XM_011525094.1:c.26_27delinsTG XP_011523396.1:p.Ala9Val
XM_011525094.2:c.26_27delinsTG XP_011523396.1:p.Ala9Val
XM_017024914.1:c.26_27delinsTG XP_016880403.1:p.Ala9Val
XM_017024915.1:c.26_27delinsTG XP_016880404.1:p.Ala9Val
XM_017024916.1:c.26_27delinsTG XP_016880405.1:p.Ala9Val
XM_017024917.1:c.26_27delinsTG XP_016880406.1:p.Ala9Val
XM_017024918.2:c.26_27delinsTG XP_016880407.1:p.Ala9Val
XM_017024919.1:c.26_27delinsTG XP_016880408.1:p.Ala9Val
XR_934513.1:n.450_451delinsTG
XR_934513.3:n.881_882delinsTG
XR_934514.1:n.450_451delinsTG
XR_934514.3:n.881_882delinsTG