Canonical Allele Identifier: CA3261180706
Community Standard Title: NM_058216.3(RAD51C):c.1105_1107delinsCTG (p.Ser369Leu)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734196_58734198delinsCTG , CM000679.2:g.58734196_58734198delinsCTG GRCh38
NC_000017.10:g.56811557_56811559delinsCTG , CM000679.1:g.56811557_56811559delinsCTG GRCh37
NC_000017.9:g.54166556_54166558delinsCTG NCBI36
NG_023199.1:g.46595_46597delinsCTG , LRG_314:g.46595_46597delinsCTG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1105_1107delinsCTG MANE Select NP_478123.1:p.Ser369Leu
ENST00000337432.9:c.1105_1107delinsCTG MANE Select ENSP00000336701.4:p.Ser369Leu
NM_058216.2:c.1105_1107delinsCTG NP_478123.1:p.Ser369Leu
NR_103872.1:n.1009_1011delinsCTG
NR_103872.2:n.980_982delinsCTG
ENST00000337432.8:c.1105_1107delinsCTG ENSP00000336701.4:p.Ser369Leu
ENST00000413590.5:c.746_748delinsCTG
ENST00000461271.6:c.*1637_*1639delinsCTG ENSP00000464056.2:n.*1637_*1639delinsCTG
ENST00000461706.1:n.292_294delinsCTG
ENST00000475762.5:c.*1741_*1743delinsCTG ENSP00000432421.1:n.*1741_*1743delinsCTG
ENST00000482007.5:c.*533_*535delinsCTG ENSP00000433332.1:n.*533_*535delinsCTG
ENST00000487525.5:c.*681_*683delinsCTG ENSP00000431637.1:n.*681_*683delinsCTG
ENST00000578151.1:n.318_320delinsCTG
ENST00000581221.5:n.620_622delinsCTG
ENST00000584804.1:c.339_341delinsCTG ENSP00000463658.1:n.339_341delinsCTG
ENST00000697680.1:c.*2069_*2071delinsCTG ENSP00000513392.1:n.*2069_*2071delinsCTG
ENST00000697681.1:c.*2266_*2268delinsCTG ENSP00000513393.1:n.*2266_*2268delinsCTG
ENST00000697683.1:c.*2041_*2043delinsCTG ENSP00000513395.1:n.*2041_*2043delinsCTG
ENST00000697685.1:c.*1802_*1804delinsCTG ENSP00000513396.1:n.*1802_*1804delinsCTG
ENST00000697686.1:c.*15_*17delinsCTG ENSP00000513397.1:n.*15_*17delinsCTG
ENST00000697689.1:c.*1519_*1521delinsCTG ENSP00000513398.1:n.*1519_*1521delinsCTG
ENST00000697690.1:c.*65_*67delinsCTG ENSP00000513399.1:n.*65_*67delinsCTG
ENST00000697691.1:c.*1077_*1079delinsCTG ENSP00000513400.1:n.*1077_*1079delinsCTG
ENST00000697692.1:c.*1117_*1119delinsCTG ENSP00000513401.1:n.*1117_*1119delinsCTG
ENST00000697694.1:c.754_756delinsCTG ENSP00000513402.1:p.Ser252Leu
ENST00000697695.1:n.1712_1714delinsCTG
XM_006722001.2:c.1108_1110delinsCTG XP_006722064.1:p.Ser370Leu
XM_006722001.4:c.1108_1110delinsCTG XP_006722064.1:p.Ser370Leu
XM_006722002.2:c.*15_*17delinsCTG XP_006722065.1:n.*15_*17delinsCTG
XM_006722002.4:c.*15_*17delinsCTG XP_006722065.1:n.*15_*17delinsCTG
XM_006722004.2:c.757_759delinsCTG XP_006722067.1:p.Ser253Leu
XM_006722004.3:c.757_759delinsCTG XP_006722067.1:p.Ser253Leu
XM_006722005.2:c.757_759delinsCTG XP_006722068.1:p.Ser253Leu
XM_006722005.3:c.757_759delinsCTG XP_006722068.1:p.Ser253Leu
XM_011525092.1:c.757_759delinsCTG XP_011523394.1:p.Ser253Leu
XM_011525092.2:c.757_759delinsCTG XP_011523394.1:p.Ser253Leu
XM_011525093.1:c.757_759delinsCTG XP_011523395.1:p.Ser253Leu
XM_011525093.2:c.757_759delinsCTG XP_011523395.1:p.Ser253Leu
XM_011525094.1:c.757_759delinsCTG XP_011523396.1:p.Ser253Leu
XM_011525094.2:c.757_759delinsCTG XP_011523396.1:p.Ser253Leu
XM_017024914.1:c.754_756delinsCTG XP_016880403.1:p.Ser252Leu
XM_017024915.1:c.754_756delinsCTG XP_016880404.1:p.Ser252Leu
XM_017024916.1:c.754_756delinsCTG XP_016880405.1:p.Ser252Leu
XM_017024917.1:c.754_756delinsCTG XP_016880406.1:p.Ser252Leu
XM_017024918.2:c.754_756delinsCTG XP_016880407.1:p.Ser252Leu
XM_017024919.1:c.*15_*17delinsCTG XP_016880408.1:n.*15_*17delinsCTG
XR_934513.1:n.1323_1325delinsCTG
XR_934513.3:n.1754_1756delinsCTG
XR_934886.1:n.149+3873_149+3875delinsCAG
XR_934886.2:n.149+3873_149+3875delinsCAG