Canonical Allele Identifier: CA3261179855
Community Standard Title: NM_058216.3(RAD51C):c.1045_1047delinsGCC (p.Thr349Ala)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734136_58734138delinsGCC , CM000679.2:g.58734136_58734138delinsGCC GRCh38
NC_000017.10:g.56811497_56811499delinsGCC , CM000679.1:g.56811497_56811499delinsGCC GRCh37
NC_000017.9:g.54166496_54166498delinsGCC NCBI36
NG_023199.1:g.46535_46537delinsGCC , LRG_314:g.46535_46537delinsGCC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1045_1047delinsGCC MANE Select NP_478123.1:p.Thr349Ala
ENST00000337432.9:c.1045_1047delinsGCC MANE Select ENSP00000336701.4:p.Thr349Ala
NM_058216.2:c.1045_1047delinsGCC NP_478123.1:p.Thr349Ala
NR_103872.1:n.949_951delinsGCC
NR_103872.2:n.920_922delinsGCC
ENST00000337432.8:c.1045_1047delinsGCC ENSP00000336701.4:p.Thr349Ala
ENST00000413590.5:c.686_688delinsGCC
ENST00000461271.6:c.*1577_*1579delinsGCC ENSP00000464056.2:n.*1577_*1579delinsGCC
ENST00000461706.1:n.232_234delinsGCC
ENST00000475762.5:c.*1681_*1683delinsGCC ENSP00000432421.1:n.*1681_*1683delinsGCC
ENST00000482007.5:c.*473_*475delinsGCC ENSP00000433332.1:n.*473_*475delinsGCC
ENST00000487525.5:c.*621_*623delinsGCC ENSP00000431637.1:n.*621_*623delinsGCC
ENST00000578151.1:n.258_260delinsGCC
ENST00000581221.5:n.560_562delinsGCC
ENST00000584804.1:c.279_281delinsGCC ENSP00000463658.1:p.Ile93_Leu94delinsMetPro
ENST00000697680.1:c.*2009_*2011delinsGCC ENSP00000513392.1:n.*2009_*2011delinsGCC
ENST00000697681.1:c.*2206_*2208delinsGCC ENSP00000513393.1:n.*2206_*2208delinsGCC
ENST00000697683.1:c.*1981_*1983delinsGCC ENSP00000513395.1:n.*1981_*1983delinsGCC
ENST00000697685.1:c.*1742_*1744delinsGCC ENSP00000513396.1:n.*1742_*1744delinsGCC
ENST00000697686.1:c.816_818delinsGCC ENSP00000513397.1:p.Ile272_Leu273delinsMetPro
ENST00000697689.1:c.*1459_*1461delinsGCC ENSP00000513398.1:n.*1459_*1461delinsGCC
ENST00000697690.1:c.*5_*7delinsGCC ENSP00000513399.1:n.*5_*7delinsGCC
ENST00000697691.1:c.*1017_*1019delinsGCC ENSP00000513400.1:n.*1017_*1019delinsGCC
ENST00000697692.1:c.*1057_*1059delinsGCC ENSP00000513401.1:n.*1057_*1059delinsGCC
ENST00000697694.1:c.694_696delinsGCC ENSP00000513402.1:p.Thr232Ala
ENST00000697695.1:n.1652_1654delinsGCC
XM_006722001.2:c.1048_1050delinsGCC XP_006722064.1:p.Thr350Ala
XM_006722001.4:c.1048_1050delinsGCC XP_006722064.1:p.Thr350Ala
XM_006722002.2:c.984_986delinsGCC XP_006722065.1:p.Ile328_Leu329delinsMetPro
XM_006722002.4:c.984_986delinsGCC XP_006722065.1:p.Ile328_Leu329delinsMetPro
XM_006722004.2:c.697_699delinsGCC XP_006722067.1:p.Thr233Ala
XM_006722004.3:c.697_699delinsGCC XP_006722067.1:p.Thr233Ala
XM_006722005.2:c.697_699delinsGCC XP_006722068.1:p.Thr233Ala
XM_006722005.3:c.697_699delinsGCC XP_006722068.1:p.Thr233Ala
XM_011525092.1:c.697_699delinsGCC XP_011523394.1:p.Thr233Ala
XM_011525092.2:c.697_699delinsGCC XP_011523394.1:p.Thr233Ala
XM_011525093.1:c.697_699delinsGCC XP_011523395.1:p.Thr233Ala
XM_011525093.2:c.697_699delinsGCC XP_011523395.1:p.Thr233Ala
XM_011525094.1:c.697_699delinsGCC XP_011523396.1:p.Thr233Ala
XM_011525094.2:c.697_699delinsGCC XP_011523396.1:p.Thr233Ala
XM_017024914.1:c.694_696delinsGCC XP_016880403.1:p.Thr232Ala
XM_017024915.1:c.694_696delinsGCC XP_016880404.1:p.Thr232Ala
XM_017024916.1:c.694_696delinsGCC XP_016880405.1:p.Thr232Ala
XM_017024917.1:c.694_696delinsGCC XP_016880406.1:p.Thr232Ala
XM_017024918.2:c.694_696delinsGCC XP_016880407.1:p.Thr232Ala
XM_017024919.1:c.633_635delinsGCC XP_016880408.1:p.Ile211_Leu212delinsMetPro
XR_934513.1:n.1263_1265delinsGCC
XR_934513.3:n.1694_1696delinsGCC
XR_934514.1:n.1266_1268delinsGCC
XR_934514.3:n.1697_1699delinsGCC
XR_934886.1:n.149+3933_149+3935delinsGGC
XR_934886.2:n.149+3933_149+3935delinsGGC