Canonical Allele Identifier: CA3261178590
Community Standard Title: NM_058216.3(RAD51C):c.973_975delinsGCC (p.Thr325Ala)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732491_58732493delinsGCC , CM000679.2:g.58732491_58732493delinsGCC GRCh38
NC_000017.10:g.56809852_56809854delinsGCC , CM000679.1:g.56809852_56809854delinsGCC GRCh37
NC_000017.9:g.54164851_54164853delinsGCC NCBI36
NG_023199.1:g.44890_44892delinsGCC , LRG_314:g.44890_44892delinsGCC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.973_975delinsGCC MANE Select NP_478123.1:p.Thr325Ala
ENST00000337432.9:c.973_975delinsGCC MANE Select ENSP00000336701.4:p.Thr325Ala
NM_058216.2:c.973_975delinsGCC NP_478123.1:p.Thr325Ala
NR_103872.1:n.877_879delinsGCC
NR_103872.2:n.848_850delinsGCC
ENST00000337432.8:c.973_975delinsGCC ENSP00000336701.4:p.Thr325Ala
ENST00000413590.5:c.614_616delinsGCC
ENST00000461271.6:c.622_624delinsGCC ENSP00000464056.2:p.Thr208Ala
ENST00000461706.1:n.160_162delinsGCC
ENST00000475762.5:c.*1609_*1611delinsGCC ENSP00000432421.1:n.*1609_*1611delinsGCC
ENST00000482007.5:c.*401_*403delinsGCC ENSP00000433332.1:n.*401_*403delinsGCC
ENST00000487525.5:c.*549_*551delinsGCC ENSP00000431637.1:n.*549_*551delinsGCC
ENST00000578151.1:n.240-1627_240-1625delinsGCC
ENST00000581221.5:n.488_490delinsGCC
ENST00000583539.5:c.973_975delinsGCC ENSP00000463121.1:p.Thr325Ala
ENST00000584617.5:c.695_697delinsGCC
ENST00000584804.1:c.207_209delinsGCC ENSP00000463658.1:p.His70Pro
ENST00000697680.1:c.*1937_*1939delinsGCC ENSP00000513392.1:n.*1937_*1939delinsGCC
ENST00000697681.1:c.*2134_*2136delinsGCC ENSP00000513393.1:n.*2134_*2136delinsGCC
ENST00000697683.1:c.*1909_*1911delinsGCC ENSP00000513395.1:n.*1909_*1911delinsGCC
ENST00000697685.1:c.*1670_*1672delinsGCC ENSP00000513396.1:n.*1670_*1672delinsGCC
ENST00000697686.1:c.744_746delinsGCC ENSP00000513397.1:p.His249Pro
ENST00000697689.1:c.*1441-1627_*1441-1625delinsGCC ENSP00000513398.1:n.*1441-1627_*1441-1625delinsGCC
ENST00000697690.1:c.905-1627_905-1625delinsGCC ENSP00000513399.1:n.905-1627_905-1625delinsGCC
ENST00000697691.1:c.*945_*947delinsGCC ENSP00000513400.1:n.*945_*947delinsGCC
ENST00000697692.1:c.*985_*987delinsGCC ENSP00000513401.1:n.*985_*987delinsGCC
ENST00000697694.1:c.622_624delinsGCC ENSP00000513402.1:p.Thr208Ala
ENST00000697695.1:n.1580_1582delinsGCC
XM_006722001.2:c.976_978delinsGCC XP_006722064.1:p.Thr326Ala
XM_006722001.4:c.976_978delinsGCC XP_006722064.1:p.Thr326Ala
XM_006722002.2:c.912_914delinsGCC XP_006722065.1:p.His305Pro
XM_006722002.4:c.912_914delinsGCC XP_006722065.1:p.His305Pro
XM_006722004.2:c.625_627delinsGCC XP_006722067.1:p.Thr209Ala
XM_006722004.3:c.625_627delinsGCC XP_006722067.1:p.Thr209Ala
XM_006722005.2:c.625_627delinsGCC XP_006722068.1:p.Thr209Ala
XM_006722005.3:c.625_627delinsGCC XP_006722068.1:p.Thr209Ala
XM_011525092.1:c.625_627delinsGCC XP_011523394.1:p.Thr209Ala
XM_011525092.2:c.625_627delinsGCC XP_011523394.1:p.Thr209Ala
XM_011525093.1:c.625_627delinsGCC XP_011523395.1:p.Thr209Ala
XM_011525093.2:c.625_627delinsGCC XP_011523395.1:p.Thr209Ala
XM_011525094.1:c.625_627delinsGCC XP_011523396.1:p.Thr209Ala
XM_011525094.2:c.625_627delinsGCC XP_011523396.1:p.Thr209Ala
XM_017024914.1:c.622_624delinsGCC XP_016880403.1:p.Thr208Ala
XM_017024915.1:c.622_624delinsGCC XP_016880404.1:p.Thr208Ala
XM_017024916.1:c.622_624delinsGCC XP_016880405.1:p.Thr208Ala
XM_017024917.1:c.622_624delinsGCC XP_016880406.1:p.Thr208Ala
XM_017024918.2:c.622_624delinsGCC XP_016880407.1:p.Thr208Ala
XM_017024919.1:c.561_563delinsGCC XP_016880408.1:p.His188Pro
XR_934513.1:n.1191_1193delinsGCC
XR_934513.3:n.1622_1624delinsGCC
XR_934514.1:n.1194_1196delinsGCC
XR_934514.3:n.1625_1627delinsGCC
XR_934886.1:n.149+5578_149+5580delinsGGC
XR_934886.2:n.149+5578_149+5580delinsGGC