Canonical Allele Identifier: CA3261180487
Community Standard Title: NM_058216.3(RAD51C):c.131_132delinsAT (p.Ser44Tyr)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692774_58692775delinsAT , CM000679.2:g.58692774_58692775delinsAT GRCh38
NC_000017.10:g.56770135_56770136delinsAT , CM000679.1:g.56770135_56770136delinsAT GRCh37
NC_000017.9:g.54125134_54125135delinsAT NCBI36
NG_023199.1:g.5173_5174delinsAT , LRG_314:g.5173_5174delinsAT
NG_047169.1:g.4305_4306delinsAT

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.131_132delinsAT MANE Select NP_478123.1:p.Ser44Tyr
ENST00000337432.9:c.131_132delinsAT MANE Select ENSP00000336701.4:p.Ser44Tyr
NM_002876.3:c.131_132delinsAT NP_002867.1:p.Ser44Tyr
NM_002876.4:c.131_132delinsAT NP_002867.1:p.Ser44Tyr
NM_058216.2:c.131_132delinsAT NP_478123.1:p.Ser44Tyr
NR_103872.1:n.202_203delinsAT
NR_103872.2:n.173_174delinsAT
NR_103873.1:n.113+89_113+90delinsAT
ENST00000337432.8:c.131_132delinsAT ENSP00000336701.4:p.Ser44Tyr
ENST00000421782.3:c.131_132delinsAT ENSP00000391450.2:p.Ser44Tyr
ENST00000461271.5:c.-207+89_-207+90delinsAT ENSP00000464056.1:n.-207+89_-207+90delinsAT
ENST00000461271.6:c.-207+89_-207+90delinsAT ENSP00000464056.2:n.-207+89_-207+90delinsAT
ENST00000475762.5:c.131_132delinsAT ENSP00000432421.1:p.Ser44Tyr
ENST00000476741.2:n.173_174delinsAT
ENST00000482007.5:c.131_132delinsAT ENSP00000433332.1:p.Ser44Tyr
ENST00000486827.1:c.131_132delinsAT ENSP00000436761.1:p.Ser44Tyr
ENST00000487525.5:c.131_132delinsAT ENSP00000431637.1:p.Ser44Tyr
ENST00000487921.5:n.57+142_57+143delinsAT
ENST00000583539.5:c.131_132delinsAT ENSP00000463121.1:p.Ser44Tyr
ENST00000584617.5:c.112_113delinsAT
ENST00000697675.1:n.202_203delinsAT
ENST00000697676.1:n.191_192delinsAT
ENST00000697677.1:n.189_190delinsAT
ENST00000697678.1:n.47+142_47+143delinsAT
ENST00000697679.1:n.182_183delinsAT
ENST00000697680.1:c.131_132delinsAT ENSP00000513392.1:p.Ser44Tyr
ENST00000697681.1:c.131_132delinsAT ENSP00000513393.1:p.Ser44Tyr
ENST00000697683.1:c.131_132delinsAT ENSP00000513395.1:p.Ser44Tyr
ENST00000697684.1:n.191_192delinsAT
ENST00000697685.1:c.131_132delinsAT ENSP00000513396.1:p.Ser44Tyr
ENST00000697686.1:c.-207+142_-207+143delinsAT ENSP00000513397.1:n.-207+142_-207+143delinsAT
ENST00000697687.1:n.177_178delinsAT
ENST00000697688.1:n.177_178delinsAT
ENST00000697689.1:c.131_132delinsAT ENSP00000513398.1:p.Ser44Tyr
ENST00000697690.1:c.131_132delinsAT ENSP00000513399.1:p.Ser44Tyr
ENST00000697691.1:c.42+89_42+90delinsAT ENSP00000513400.1:n.42+89_42+90delinsAT
ENST00000697692.1:c.131_132delinsAT ENSP00000513401.1:p.Ser44Tyr
ENST00000697693.1:n.44_45delinsAT
XM_006722001.2:c.131_132delinsAT XP_006722064.1:p.Ser44Tyr
XM_006722001.4:c.131_132delinsAT XP_006722064.1:p.Ser44Tyr
XM_006722002.2:c.131_132delinsAT XP_006722065.1:p.Ser44Tyr
XM_006722002.4:c.131_132delinsAT XP_006722065.1:p.Ser44Tyr
XM_006722004.2:c.-207+89_-207+90delinsAT XP_006722067.1:n.-207+89_-207+90delinsAT
XM_006722004.3:c.-207+89_-207+90delinsAT XP_006722067.1:n.-207+89_-207+90delinsAT
XM_006722005.2:c.-207+142_-207+143delinsAT XP_006722068.1:n.-207+142_-207+143delinsAT
XM_006722005.3:c.-207+142_-207+143delinsAT XP_006722068.1:n.-207+142_-207+143delinsAT
XM_011525092.1:c.-507+89_-507+90delinsAT XP_011523394.1:n.-507+89_-507+90delinsAT
XM_011525092.2:c.-507+89_-507+90delinsAT XP_011523394.1:n.-507+89_-507+90delinsAT
XM_011525093.1:c.-668+89_-668+90delinsAT XP_011523395.1:n.-668+89_-668+90delinsAT
XM_011525093.2:c.-668+89_-668+90delinsAT XP_011523395.1:n.-668+89_-668+90delinsAT
XM_017024914.1:c.-207+89_-207+90delinsAT XP_016880403.1:n.-207+89_-207+90delinsAT
XM_017024916.1:c.-507+89_-507+90delinsAT XP_016880405.1:n.-507+89_-507+90delinsAT
XM_017024917.1:c.-207+142_-207+143delinsAT XP_016880406.1:n.-207+142_-207+143delinsAT
XM_017024918.2:c.-392_-391delinsAT XP_016880407.1:n.-392_-391delinsAT
XM_017024919.1:c.-668+89_-668+90delinsAT XP_016880408.1:n.-668+89_-668+90delinsAT
XR_934513.1:n.204_205delinsAT
XR_934513.3:n.635_636delinsAT
XR_934514.1:n.204_205delinsAT
XR_934514.3:n.635_636delinsAT