Canonical Allele Identifier: CA3261178764
Community Standard Title: NM_058216.3(RAD51C):c.862_864delinsGCC (p.Thr288Ala)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58720770_58720772delinsGCC , CM000679.2:g.58720770_58720772delinsGCC GRCh38
NC_000017.10:g.56798131_56798133delinsGCC , CM000679.1:g.56798131_56798133delinsGCC GRCh37
NC_000017.9:g.54153130_54153132delinsGCC NCBI36
NG_023199.1:g.33169_33171delinsGCC , LRG_314:g.33169_33171delinsGCC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.862_864delinsGCC MANE Select NP_478123.1:p.Thr288Ala
ENST00000337432.9:c.862_864delinsGCC MANE Select ENSP00000336701.4:p.Thr288Ala
NM_058216.2:c.862_864delinsGCC NP_478123.1:p.Thr288Ala
NR_103872.1:n.766_768delinsGCC
NR_103872.2:n.737_739delinsGCC
ENST00000337432.8:c.862_864delinsGCC ENSP00000336701.4:p.Thr288Ala
ENST00000413590.5:c.500_502delinsGCC
ENST00000461271.6:c.511_513delinsGCC ENSP00000464056.2:p.Thr171Ala
ENST00000475762.5:c.*1541-3270_*1541-3268delinsGCC ENSP00000432421.1:n.*1541-3270_*1541-3268delinsGCC
ENST00000482007.5:c.*290_*292delinsGCC ENSP00000433332.1:n.*290_*292delinsGCC
ENST00000487525.5:c.*435_*437delinsGCC ENSP00000431637.1:n.*435_*437delinsGCC
ENST00000578151.1:n.197_199delinsGCC
ENST00000581221.5:n.377_379delinsGCC
ENST00000583539.5:c.862_864delinsGCC ENSP00000463121.1:p.Thr288Ala
ENST00000584617.5:c.584_586delinsGCC
ENST00000584804.1:c.157_159delinsGCC ENSP00000463658.1:p.Thr53Ala
ENST00000697678.1:n.764_766delinsGCC
ENST00000697679.1:n.1936_1938delinsGCC
ENST00000697680.1:c.*1826_*1828delinsGCC ENSP00000513392.1:n.*1826_*1828delinsGCC
ENST00000697681.1:c.*2023_*2025delinsGCC ENSP00000513393.1:n.*2023_*2025delinsGCC
ENST00000697683.1:c.*1726_*1728delinsGCC ENSP00000513395.1:n.*1726_*1728delinsGCC
ENST00000697684.1:n.922_924delinsGCC
ENST00000697685.1:c.*1559_*1561delinsGCC ENSP00000513396.1:n.*1559_*1561delinsGCC
ENST00000697686.1:c.511_513delinsGCC ENSP00000513397.1:p.Thr171Ala
ENST00000697687.1:n.741_743delinsGCC
ENST00000697688.1:n.908_910delinsGCC
ENST00000697689.1:c.*1398_*1400delinsGCC ENSP00000513398.1:n.*1398_*1400delinsGCC
ENST00000697690.1:c.862_864delinsGCC ENSP00000513399.1:p.Thr288Ala
ENST00000697691.1:c.*834_*836delinsGCC ENSP00000513400.1:n.*834_*836delinsGCC
ENST00000697692.1:c.*874_*876delinsGCC ENSP00000513401.1:n.*874_*876delinsGCC
ENST00000697694.1:c.511_513delinsGCC ENSP00000513402.1:p.Thr171Ala
ENST00000697695.1:n.1469_1471delinsGCC
XM_006722001.2:c.862_864delinsGCC XP_006722064.1:p.Thr288Ala
XM_006722001.4:c.862_864delinsGCC XP_006722064.1:p.Thr288Ala
XM_006722002.2:c.862_864delinsGCC XP_006722065.1:p.Thr288Ala
XM_006722002.4:c.862_864delinsGCC XP_006722065.1:p.Thr288Ala
XM_006722004.2:c.511_513delinsGCC XP_006722067.1:p.Thr171Ala
XM_006722004.3:c.511_513delinsGCC XP_006722067.1:p.Thr171Ala
XM_006722005.2:c.511_513delinsGCC XP_006722068.1:p.Thr171Ala
XM_006722005.3:c.511_513delinsGCC XP_006722068.1:p.Thr171Ala
XM_011525092.1:c.511_513delinsGCC XP_011523394.1:p.Thr171Ala
XM_011525092.2:c.511_513delinsGCC XP_011523394.1:p.Thr171Ala
XM_011525093.1:c.511_513delinsGCC XP_011523395.1:p.Thr171Ala
XM_011525093.2:c.511_513delinsGCC XP_011523395.1:p.Thr171Ala
XM_011525094.1:c.511_513delinsGCC XP_011523396.1:p.Thr171Ala
XM_011525094.2:c.511_513delinsGCC XP_011523396.1:p.Thr171Ala
XM_017024914.1:c.511_513delinsGCC XP_016880403.1:p.Thr171Ala
XM_017024915.1:c.511_513delinsGCC XP_016880404.1:p.Thr171Ala
XM_017024916.1:c.511_513delinsGCC XP_016880405.1:p.Thr171Ala
XM_017024917.1:c.511_513delinsGCC XP_016880406.1:p.Thr171Ala
XM_017024918.2:c.511_513delinsGCC XP_016880407.1:p.Thr171Ala
XM_017024919.1:c.511_513delinsGCC XP_016880408.1:p.Thr171Ala
XR_934513.1:n.1080_1082delinsGCC
XR_934513.3:n.1511_1513delinsGCC
XR_934514.1:n.1080_1082delinsGCC
XR_934514.3:n.1511_1513delinsGCC