Canonical Allele Identifier: CA3261179302
Community Standard Title: NM_058216.3(RAD51C):c.1015_1017delinsAGC (p.Phe339Ser)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732533_58732535delinsAGC , CM000679.2:g.58732533_58732535delinsAGC GRCh38
NC_000017.10:g.56809894_56809896delinsAGC , CM000679.1:g.56809894_56809896delinsAGC GRCh37
NC_000017.9:g.54164893_54164895delinsAGC NCBI36
NG_023199.1:g.44932_44934delinsAGC , LRG_314:g.44932_44934delinsAGC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1015_1017delinsAGC MANE Select NP_478123.1:p.Phe339Ser
ENST00000337432.9:c.1015_1017delinsAGC MANE Select ENSP00000336701.4:p.Phe339Ser
NM_058216.2:c.1015_1017delinsAGC NP_478123.1:p.Phe339Ser
NR_103872.1:n.919_921delinsAGC
NR_103872.2:n.890_892delinsAGC
ENST00000337432.8:c.1015_1017delinsAGC ENSP00000336701.4:p.Phe339Ser
ENST00000413590.5:c.656_658delinsAGC
ENST00000461271.6:c.664_666delinsAGC ENSP00000464056.2:p.Phe222Ser
ENST00000461706.1:n.202_204delinsAGC
ENST00000475762.5:c.*1651_*1653delinsAGC ENSP00000432421.1:n.*1651_*1653delinsAGC
ENST00000482007.5:c.*443_*445delinsAGC ENSP00000433332.1:n.*443_*445delinsAGC
ENST00000487525.5:c.*591_*593delinsAGC ENSP00000431637.1:n.*591_*593delinsAGC
ENST00000578151.1:n.240-1585_240-1583delinsAGC
ENST00000581221.5:n.530_532delinsAGC
ENST00000583539.5:c.1015_1017delinsAGC ENSP00000463121.1:p.Phe339Ser
ENST00000584804.1:c.249_251delinsAGC ENSP00000463658.1:p.Cys83Ter
ENST00000697680.1:c.*1979_*1981delinsAGC ENSP00000513392.1:n.*1979_*1981delinsAGC
ENST00000697681.1:c.*2176_*2178delinsAGC ENSP00000513393.1:n.*2176_*2178delinsAGC
ENST00000697683.1:c.*1951_*1953delinsAGC ENSP00000513395.1:n.*1951_*1953delinsAGC
ENST00000697685.1:c.*1712_*1714delinsAGC ENSP00000513396.1:n.*1712_*1714delinsAGC
ENST00000697686.1:c.786_788delinsAGC ENSP00000513397.1:p.Cys262Ter
ENST00000697689.1:c.*1441-1585_*1441-1583delinsAGC ENSP00000513398.1:n.*1441-1585_*1441-1583delinsAGC
ENST00000697690.1:c.905-1585_905-1583delinsAGC ENSP00000513399.1:n.905-1585_905-1583delinsAGC
ENST00000697691.1:c.*987_*989delinsAGC ENSP00000513400.1:n.*987_*989delinsAGC
ENST00000697692.1:c.*1027_*1029delinsAGC ENSP00000513401.1:n.*1027_*1029delinsAGC
ENST00000697694.1:c.664_666delinsAGC ENSP00000513402.1:p.Phe222Ser
ENST00000697695.1:n.1622_1624delinsAGC
XM_006722001.2:c.1018_1020delinsAGC XP_006722064.1:p.Phe340Ser
XM_006722001.4:c.1018_1020delinsAGC XP_006722064.1:p.Phe340Ser
XM_006722002.2:c.954_956delinsAGC XP_006722065.1:p.Cys318Ter
XM_006722002.4:c.954_956delinsAGC XP_006722065.1:p.Cys318Ter
XM_006722004.2:c.667_669delinsAGC XP_006722067.1:p.Phe223Ser
XM_006722004.3:c.667_669delinsAGC XP_006722067.1:p.Phe223Ser
XM_006722005.2:c.667_669delinsAGC XP_006722068.1:p.Phe223Ser
XM_006722005.3:c.667_669delinsAGC XP_006722068.1:p.Phe223Ser
XM_011525092.1:c.667_669delinsAGC XP_011523394.1:p.Phe223Ser
XM_011525092.2:c.667_669delinsAGC XP_011523394.1:p.Phe223Ser
XM_011525093.1:c.667_669delinsAGC XP_011523395.1:p.Phe223Ser
XM_011525093.2:c.667_669delinsAGC XP_011523395.1:p.Phe223Ser
XM_011525094.1:c.667_669delinsAGC XP_011523396.1:p.Phe223Ser
XM_011525094.2:c.667_669delinsAGC XP_011523396.1:p.Phe223Ser
XM_017024914.1:c.664_666delinsAGC XP_016880403.1:p.Phe222Ser
XM_017024915.1:c.664_666delinsAGC XP_016880404.1:p.Phe222Ser
XM_017024916.1:c.664_666delinsAGC XP_016880405.1:p.Phe222Ser
XM_017024917.1:c.664_666delinsAGC XP_016880406.1:p.Phe222Ser
XM_017024918.2:c.664_666delinsAGC XP_016880407.1:p.Phe222Ser
XM_017024919.1:c.603_605delinsAGC XP_016880408.1:p.Cys201Ter
XR_934513.1:n.1233_1235delinsAGC
XR_934513.3:n.1664_1666delinsAGC
XR_934514.1:n.1236_1238delinsAGC
XR_934514.3:n.1667_1669delinsAGC
XR_934886.1:n.149+5536_149+5538delinsGCT
XR_934886.2:n.149+5536_149+5538delinsGCT