Canonical Allele Identifier: CA3261180821
Community Standard Title: NM_058216.3(RAD51C):c.1118_1119delinsCC (p.Glu373Ala)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734209_58734210delinsCC , CM000679.2:g.58734209_58734210delinsCC GRCh38
NC_000017.10:g.56811570_56811571delinsCC , CM000679.1:g.56811570_56811571delinsCC GRCh37
NC_000017.9:g.54166569_54166570delinsCC NCBI36
NG_023199.1:g.46608_46609delinsCC , LRG_314:g.46608_46609delinsCC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1118_1119delinsCC MANE Select NP_478123.1:p.Glu373Ala
ENST00000337432.9:c.1118_1119delinsCC MANE Select ENSP00000336701.4:p.Glu373Ala
NM_058216.2:c.1118_1119delinsCC NP_478123.1:p.Glu373Ala
NR_103872.1:n.1022_1023delinsCC
NR_103872.2:n.993_994delinsCC
ENST00000337432.8:c.1118_1119delinsCC ENSP00000336701.4:p.Glu373Ala
ENST00000413590.5:c.759_760delinsCC
ENST00000461271.6:c.*1650_*1651delinsCC ENSP00000464056.2:n.*1650_*1651delinsCC
ENST00000461706.1:n.305_306delinsCC
ENST00000475762.5:c.*1754_*1755delinsCC ENSP00000432421.1:n.*1754_*1755delinsCC
ENST00000482007.5:c.*546_*547delinsCC ENSP00000433332.1:n.*546_*547delinsCC
ENST00000487525.5:c.*694_*695delinsCC ENSP00000431637.1:n.*694_*695delinsCC
ENST00000578151.1:n.331_332delinsCC
ENST00000581221.5:n.633_634delinsCC
ENST00000584804.1:c.352_353delinsCC ENSP00000463658.1:n.352_353delinsCC
ENST00000697680.1:c.*2082_*2083delinsCC ENSP00000513392.1:n.*2082_*2083delinsCC
ENST00000697681.1:c.*2279_*2280delinsCC ENSP00000513393.1:n.*2279_*2280delinsCC
ENST00000697683.1:c.*2054_*2055delinsCC ENSP00000513395.1:n.*2054_*2055delinsCC
ENST00000697685.1:c.*1815_*1816delinsCC ENSP00000513396.1:n.*1815_*1816delinsCC
ENST00000697686.1:c.*28_*29delinsCC ENSP00000513397.1:n.*28_*29delinsCC
ENST00000697689.1:c.*1532_*1533delinsCC ENSP00000513398.1:n.*1532_*1533delinsCC
ENST00000697690.1:c.*78_*79delinsCC ENSP00000513399.1:n.*78_*79delinsCC
ENST00000697691.1:c.*1090_*1091delinsCC ENSP00000513400.1:n.*1090_*1091delinsCC
ENST00000697692.1:c.*1130_*1131delinsCC ENSP00000513401.1:n.*1130_*1131delinsCC
ENST00000697694.1:c.767_768delinsCC ENSP00000513402.1:p.Glu256Ala
ENST00000697695.1:n.1725_1726delinsCC
XM_006722001.2:c.1121_1122delinsCC XP_006722064.1:p.Glu374Ala
XM_006722001.4:c.1121_1122delinsCC XP_006722064.1:p.Glu374Ala
XM_006722002.2:c.*28_*29delinsCC XP_006722065.1:n.*28_*29delinsCC
XM_006722002.4:c.*28_*29delinsCC XP_006722065.1:n.*28_*29delinsCC
XM_006722004.2:c.770_771delinsCC XP_006722067.1:p.Glu257Ala
XM_006722004.3:c.770_771delinsCC XP_006722067.1:p.Glu257Ala
XM_006722005.2:c.770_771delinsCC XP_006722068.1:p.Glu257Ala
XM_006722005.3:c.770_771delinsCC XP_006722068.1:p.Glu257Ala
XM_011525092.1:c.770_771delinsCC XP_011523394.1:p.Glu257Ala
XM_011525092.2:c.770_771delinsCC XP_011523394.1:p.Glu257Ala
XM_011525093.1:c.770_771delinsCC XP_011523395.1:p.Glu257Ala
XM_011525093.2:c.770_771delinsCC XP_011523395.1:p.Glu257Ala
XM_011525094.1:c.770_771delinsCC XP_011523396.1:p.Glu257Ala
XM_011525094.2:c.770_771delinsCC XP_011523396.1:p.Glu257Ala
XM_017024914.1:c.767_768delinsCC XP_016880403.1:p.Glu256Ala
XM_017024915.1:c.767_768delinsCC XP_016880404.1:p.Glu256Ala
XM_017024916.1:c.767_768delinsCC XP_016880405.1:p.Glu256Ala
XM_017024917.1:c.767_768delinsCC XP_016880406.1:p.Glu256Ala
XM_017024918.2:c.767_768delinsCC XP_016880407.1:p.Glu256Ala
XM_017024919.1:c.*28_*29delinsCC XP_016880408.1:n.*28_*29delinsCC
XR_934513.1:n.1336_1337delinsCC
XR_934513.3:n.1767_1768delinsCC
XR_934886.1:n.149+3861_149+3862delinsGG
XR_934886.2:n.149+3861_149+3862delinsGG