Canonical Allele Identifier: CA3057243182
Community Standard Title: NM_058216.3(RAD51C):c.972_973delinsGC (p.Thr325Pro)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732490_58732491delinsGC , CM000679.2:g.58732490_58732491delinsGC GRCh38
NC_000017.10:g.56809851_56809852delinsGC , CM000679.1:g.56809851_56809852delinsGC GRCh37
NC_000017.9:g.54164850_54164851delinsGC NCBI36
NG_023199.1:g.44889_44890delinsGC , LRG_314:g.44889_44890delinsGC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.972_973delinsGC MANE Select NP_478123.1:p.Thr325Pro
ENST00000337432.9:c.972_973delinsGC MANE Select ENSP00000336701.4:p.Thr325Pro
NM_058216.2:c.972_973delinsGC NP_478123.1:p.Thr325Pro
NR_103872.1:n.876_877delinsGC
NR_103872.2:n.847_848delinsGC
ENST00000337432.8:c.972_973delinsGC ENSP00000336701.4:p.Thr325Pro
ENST00000413590.5:c.613_614delinsGC
ENST00000461271.6:c.621_622delinsGC ENSP00000464056.2:p.Thr208Pro
ENST00000461706.1:n.159_160delinsGC
ENST00000475762.5:c.*1608_*1609delinsGC ENSP00000432421.1:n.*1608_*1609delinsGC
ENST00000482007.5:c.*400_*401delinsGC ENSP00000433332.1:n.*400_*401delinsGC
ENST00000487525.5:c.*548_*549delinsGC ENSP00000431637.1:n.*548_*549delinsGC
ENST00000578151.1:n.240-1628_240-1627delinsGC
ENST00000581221.5:n.487_488delinsGC
ENST00000583539.5:c.972_973delinsGC ENSP00000463121.1:p.Thr325Pro
ENST00000584617.5:c.694_695delinsGC
ENST00000584804.1:c.206_207delinsGC ENSP00000463658.1:p.Gln69Arg
ENST00000697680.1:c.*1936_*1937delinsGC ENSP00000513392.1:n.*1936_*1937delinsGC
ENST00000697681.1:c.*2133_*2134delinsGC ENSP00000513393.1:n.*2133_*2134delinsGC
ENST00000697683.1:c.*1908_*1909delinsGC ENSP00000513395.1:n.*1908_*1909delinsGC
ENST00000697685.1:c.*1669_*1670delinsGC ENSP00000513396.1:n.*1669_*1670delinsGC
ENST00000697686.1:c.743_744delinsGC ENSP00000513397.1:p.Gln248Arg
ENST00000697689.1:c.*1441-1628_*1441-1627delinsGC ENSP00000513398.1:n.*1441-1628_*1441-1627delinsGC
ENST00000697690.1:c.905-1628_905-1627delinsGC ENSP00000513399.1:n.905-1628_905-1627delinsGC
ENST00000697691.1:c.*944_*945delinsGC ENSP00000513400.1:n.*944_*945delinsGC
ENST00000697692.1:c.*984_*985delinsGC ENSP00000513401.1:n.*984_*985delinsGC
ENST00000697694.1:c.621_622delinsGC ENSP00000513402.1:p.Thr208Pro
ENST00000697695.1:n.1579_1580delinsGC
XM_006722001.2:c.975_976delinsGC XP_006722064.1:p.Thr326Pro
XM_006722001.4:c.975_976delinsGC XP_006722064.1:p.Thr326Pro
XM_006722002.2:c.911_912delinsGC XP_006722065.1:p.Gln304Arg
XM_006722002.4:c.911_912delinsGC XP_006722065.1:p.Gln304Arg
XM_006722004.2:c.624_625delinsGC XP_006722067.1:p.Thr209Pro
XM_006722004.3:c.624_625delinsGC XP_006722067.1:p.Thr209Pro
XM_006722005.2:c.624_625delinsGC XP_006722068.1:p.Thr209Pro
XM_006722005.3:c.624_625delinsGC XP_006722068.1:p.Thr209Pro
XM_011525092.1:c.624_625delinsGC XP_011523394.1:p.Thr209Pro
XM_011525092.2:c.624_625delinsGC XP_011523394.1:p.Thr209Pro
XM_011525093.1:c.624_625delinsGC XP_011523395.1:p.Thr209Pro
XM_011525093.2:c.624_625delinsGC XP_011523395.1:p.Thr209Pro
XM_011525094.1:c.624_625delinsGC XP_011523396.1:p.Thr209Pro
XM_011525094.2:c.624_625delinsGC XP_011523396.1:p.Thr209Pro
XM_017024914.1:c.621_622delinsGC XP_016880403.1:p.Thr208Pro
XM_017024915.1:c.621_622delinsGC XP_016880404.1:p.Thr208Pro
XM_017024916.1:c.621_622delinsGC XP_016880405.1:p.Thr208Pro
XM_017024917.1:c.621_622delinsGC XP_016880406.1:p.Thr208Pro
XM_017024918.2:c.621_622delinsGC XP_016880407.1:p.Thr208Pro
XM_017024919.1:c.560_561delinsGC XP_016880408.1:p.Gln187Arg
XR_934513.1:n.1190_1191delinsGC
XR_934513.3:n.1621_1622delinsGC
XR_934514.1:n.1193_1194delinsGC
XR_934514.3:n.1624_1625delinsGC
XR_934886.1:n.149+5580_149+5581delinsGC
XR_934886.2:n.149+5580_149+5581delinsGC