Canonical Allele Identifier: CA3261179230
Community Standard Title: NM_058216.3(RAD51C):c.892_894delinsATC (p.Val298Ile)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58720800_58720802delinsATC , CM000679.2:g.58720800_58720802delinsATC GRCh38
NC_000017.10:g.56798161_56798163delinsATC , CM000679.1:g.56798161_56798163delinsATC GRCh37
NC_000017.9:g.54153160_54153162delinsATC NCBI36
NG_023199.1:g.33199_33201delinsATC , LRG_314:g.33199_33201delinsATC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.892_894delinsATC MANE Select NP_478123.1:p.Val298Ile
ENST00000337432.9:c.892_894delinsATC MANE Select ENSP00000336701.4:p.Val298Ile
NM_058216.2:c.892_894delinsATC NP_478123.1:p.Val298Ile
NR_103872.1:n.796_798delinsATC
NR_103872.2:n.767_769delinsATC
ENST00000337432.8:c.892_894delinsATC ENSP00000336701.4:p.Val298Ile
ENST00000413590.5:c.530_532delinsATC
ENST00000461271.6:c.541_543delinsATC ENSP00000464056.2:p.Val181Ile
ENST00000475762.5:c.*1541-3240_*1541-3238delinsATC ENSP00000432421.1:n.*1541-3240_*1541-3238delinsATC
ENST00000482007.5:c.*320_*322delinsATC ENSP00000433332.1:n.*320_*322delinsATC
ENST00000487525.5:c.*465_*467delinsATC ENSP00000431637.1:n.*465_*467delinsATC
ENST00000578151.1:n.227_229delinsATC
ENST00000581221.5:n.407_409delinsATC
ENST00000583539.5:c.892_894delinsATC ENSP00000463121.1:p.Val298Ile
ENST00000584617.5:c.614_616delinsATC
ENST00000584804.1:c.187_189delinsATC ENSP00000463658.1:p.Val63Ile
ENST00000697678.1:n.794_796delinsATC
ENST00000697679.1:n.1966_1968delinsATC
ENST00000697680.1:c.*1856_*1858delinsATC ENSP00000513392.1:n.*1856_*1858delinsATC
ENST00000697681.1:c.*2053_*2055delinsATC ENSP00000513393.1:n.*2053_*2055delinsATC
ENST00000697683.1:c.*1756_*1758delinsATC ENSP00000513395.1:n.*1756_*1758delinsATC
ENST00000697684.1:n.952_954delinsATC
ENST00000697685.1:c.*1589_*1591delinsATC ENSP00000513396.1:n.*1589_*1591delinsATC
ENST00000697686.1:c.541_543delinsATC ENSP00000513397.1:p.Val181Ile
ENST00000697687.1:n.771_773delinsATC
ENST00000697688.1:n.938_940delinsATC
ENST00000697689.1:c.*1428_*1430delinsATC ENSP00000513398.1:n.*1428_*1430delinsATC
ENST00000697690.1:c.892_894delinsATC ENSP00000513399.1:p.Val298Ile
ENST00000697691.1:c.*864_*866delinsATC ENSP00000513400.1:n.*864_*866delinsATC
ENST00000697692.1:c.*904_*906delinsATC ENSP00000513401.1:n.*904_*906delinsATC
ENST00000697694.1:c.541_543delinsATC ENSP00000513402.1:p.Val181Ile
ENST00000697695.1:n.1499_1501delinsATC
XM_006722001.2:c.892_894delinsATC XP_006722064.1:p.Val298Ile
XM_006722001.4:c.892_894delinsATC XP_006722064.1:p.Val298Ile
XM_006722002.2:c.892_894delinsATC XP_006722065.1:p.Val298Ile
XM_006722002.4:c.892_894delinsATC XP_006722065.1:p.Val298Ile
XM_006722004.2:c.541_543delinsATC XP_006722067.1:p.Val181Ile
XM_006722004.3:c.541_543delinsATC XP_006722067.1:p.Val181Ile
XM_006722005.2:c.541_543delinsATC XP_006722068.1:p.Val181Ile
XM_006722005.3:c.541_543delinsATC XP_006722068.1:p.Val181Ile
XM_011525092.1:c.541_543delinsATC XP_011523394.1:p.Val181Ile
XM_011525092.2:c.541_543delinsATC XP_011523394.1:p.Val181Ile
XM_011525093.1:c.541_543delinsATC XP_011523395.1:p.Val181Ile
XM_011525093.2:c.541_543delinsATC XP_011523395.1:p.Val181Ile
XM_011525094.1:c.541_543delinsATC XP_011523396.1:p.Val181Ile
XM_011525094.2:c.541_543delinsATC XP_011523396.1:p.Val181Ile
XM_017024914.1:c.541_543delinsATC XP_016880403.1:p.Val181Ile
XM_017024915.1:c.541_543delinsATC XP_016880404.1:p.Val181Ile
XM_017024916.1:c.541_543delinsATC XP_016880405.1:p.Val181Ile
XM_017024917.1:c.541_543delinsATC XP_016880406.1:p.Val181Ile
XM_017024918.2:c.541_543delinsATC XP_016880407.1:p.Val181Ile
XM_017024919.1:c.541_543delinsATC XP_016880408.1:p.Val181Ile
XR_934513.1:n.1110_1112delinsATC
XR_934513.3:n.1541_1543delinsATC
XR_934514.1:n.1110_1112delinsATC
XR_934514.3:n.1541_1543delinsATC