Canonical Allele Identifier: CA3261180808
Community Standard Title: NM_058216.3(RAD51C):c.449_450delinsAG (p.Gly150Glu)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58696737_58696738delinsAG , CM000679.2:g.58696737_58696738delinsAG GRCh38
NC_000017.10:g.56774098_56774099delinsAG , CM000679.1:g.56774098_56774099delinsAG GRCh37
NC_000017.9:g.54129097_54129098delinsAG NCBI36
NG_023199.1:g.9136_9137delinsAG , LRG_314:g.9136_9137delinsAG
NG_047169.1:g.342_343delinsCT

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.449_450delinsAG MANE Select NP_478123.1:p.Gly150Glu
ENST00000337432.9:c.449_450delinsAG MANE Select ENSP00000336701.4:p.Gly150Glu
NM_058216.2:c.449_450delinsAG NP_478123.1:p.Gly150Glu
NR_103872.1:n.475+1548_475+1549delinsAG
NR_103872.2:n.446+1548_446+1549delinsAG
ENST00000337432.8:c.449_450delinsAG ENSP00000336701.4:p.Gly150Glu
ENST00000413590.5:c.87_88delinsAG
ENST00000425173.5:c.245_246delinsAG ENSP00000407282.1:p.Gly82Glu
ENST00000461271.5:c.98_99delinsAG ENSP00000464056.1:p.Gly33Glu
ENST00000461271.6:c.98_99delinsAG ENSP00000464056.2:p.Gly33Glu
ENST00000475762.5:c.*1152_*1153delinsAG ENSP00000432421.1:n.*1152_*1153delinsAG
ENST00000482007.5:c.404+1548_404+1549delinsAG ENSP00000433332.1:n.404+1548_404+1549delinsAG
ENST00000487525.5:c.404+1548_404+1549delinsAG ENSP00000431637.1:n.404+1548_404+1549delinsAG
ENST00000487921.5:n.361_362delinsAG
ENST00000583539.5:c.449_450delinsAG ENSP00000463121.1:p.Gly150Glu
ENST00000584617.5:c.171_172delinsAG
ENST00000622327.4:c.185_186delinsAG ENSP00000482326.1:p.Gly62Glu
ENST00000697675.1:n.3046_3047delinsAG
ENST00000697676.1:n.509_510delinsAG
ENST00000697677.1:n.1530_1531delinsAG
ENST00000697678.1:n.351_352delinsAG
ENST00000697679.1:n.1523_1524delinsAG
ENST00000697680.1:c.*1313_*1314delinsAG ENSP00000513392.1:n.*1313_*1314delinsAG
ENST00000697681.1:c.*1340_*1341delinsAG ENSP00000513393.1:n.*1340_*1341delinsAG
ENST00000697683.1:c.*1313_*1314delinsAG ENSP00000513395.1:n.*1313_*1314delinsAG
ENST00000697684.1:n.509_510delinsAG
ENST00000697685.1:c.*1268+1548_*1268+1549delinsAG ENSP00000513396.1:n.*1268+1548_*1268+1549delinsAG
ENST00000697686.1:c.98_99delinsAG ENSP00000513397.1:p.Gly33Glu
ENST00000697687.1:n.450+1548_450+1549delinsAG
ENST00000697688.1:n.495_496delinsAG
ENST00000697689.1:c.*1107+1548_*1107+1549delinsAG ENSP00000513398.1:n.*1107+1548_*1107+1549delinsAG
ENST00000697690.1:c.449_450delinsAG ENSP00000513399.1:p.Gly150Glu
ENST00000697691.1:c.*421_*422delinsAG ENSP00000513400.1:n.*421_*422delinsAG
ENST00000697692.1:c.*461_*462delinsAG ENSP00000513401.1:n.*461_*462delinsAG
ENST00000697694.1:c.98_99delinsAG ENSP00000513402.1:p.Gly33Glu
ENST00000697695.1:n.1056_1057delinsAG
XM_006722001.2:c.449_450delinsAG XP_006722064.1:p.Gly150Glu
XM_006722001.4:c.449_450delinsAG XP_006722064.1:p.Gly150Glu
XM_006722002.2:c.449_450delinsAG XP_006722065.1:p.Gly150Glu
XM_006722002.4:c.449_450delinsAG XP_006722065.1:p.Gly150Glu
XM_006722004.2:c.98_99delinsAG XP_006722067.1:p.Gly33Glu
XM_006722004.3:c.98_99delinsAG XP_006722067.1:p.Gly33Glu
XM_006722005.2:c.98_99delinsAG XP_006722068.1:p.Gly33Glu
XM_006722005.3:c.98_99delinsAG XP_006722068.1:p.Gly33Glu
XM_011525092.1:c.98_99delinsAG XP_011523394.1:p.Gly33Glu
XM_011525092.2:c.98_99delinsAG XP_011523394.1:p.Gly33Glu
XM_011525093.1:c.98_99delinsAG XP_011523395.1:p.Gly33Glu
XM_011525093.2:c.98_99delinsAG XP_011523395.1:p.Gly33Glu
XM_011525094.1:c.98_99delinsAG XP_011523396.1:p.Gly33Glu
XM_011525094.2:c.98_99delinsAG XP_011523396.1:p.Gly33Glu
XM_017024914.1:c.98_99delinsAG XP_016880403.1:p.Gly33Glu
XM_017024915.1:c.98_99delinsAG XP_016880404.1:p.Gly33Glu
XM_017024916.1:c.98_99delinsAG XP_016880405.1:p.Gly33Glu
XM_017024917.1:c.98_99delinsAG XP_016880406.1:p.Gly33Glu
XM_017024918.2:c.98_99delinsAG XP_016880407.1:p.Gly33Glu
XM_017024919.1:c.98_99delinsAG XP_016880408.1:p.Gly33Glu
XR_934513.1:n.522_523delinsAG
XR_934513.3:n.953_954delinsAG
XR_934514.1:n.522_523delinsAG
XR_934514.3:n.953_954delinsAG