Canonical Allele Identifier: CA3057228232
Community Standard Title: NM_058216.3(RAD51C):c.804_805delinsGC (p.Met269Leu)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709957_58709958delinsGC , CM000679.2:g.58709957_58709958delinsGC GRCh38
NC_000017.10:g.56787318_56787319delinsGC , CM000679.1:g.56787318_56787319delinsGC GRCh37
NC_000017.9:g.54142317_54142318delinsGC NCBI36
NG_023199.1:g.22356_22357delinsGC , LRG_314:g.22356_22357delinsGC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.804_805delinsGC MANE Select NP_478123.1:p.Met269Leu
ENST00000337432.9:c.804_805delinsGC MANE Select ENSP00000336701.4:p.Met269Leu
NM_058216.2:c.804_805delinsGC NP_478123.1:p.Met269Leu
NR_103872.1:n.708_709delinsGC
NR_103872.2:n.679_680delinsGC
ENST00000337432.8:c.804_805delinsGC ENSP00000336701.4:p.Met269Leu
ENST00000413590.5:c.442_443delinsGC
ENST00000461271.6:c.453_454delinsGC ENSP00000464056.2:p.Met152Leu
ENST00000475762.5:c.*1507_*1508delinsGC ENSP00000432421.1:n.*1507_*1508delinsGC
ENST00000482007.5:c.*232_*233delinsGC ENSP00000433332.1:n.*232_*233delinsGC
ENST00000487525.5:c.*377_*378delinsGC ENSP00000431637.1:n.*377_*378delinsGC
ENST00000578151.1:n.139_140delinsGC
ENST00000581221.5:n.319_320delinsGC
ENST00000583539.5:c.804_805delinsGC ENSP00000463121.1:p.Met269Leu
ENST00000584617.5:c.526_527delinsGC
ENST00000584804.1:c.99_100delinsGC ENSP00000463658.1:p.Met34Leu
ENST00000697678.1:n.706_707delinsGC
ENST00000697679.1:n.1878_1879delinsGC
ENST00000697680.1:c.*1668_*1669delinsGC ENSP00000513392.1:n.*1668_*1669delinsGC
ENST00000697681.1:c.*1965_*1966delinsGC ENSP00000513393.1:n.*1965_*1966delinsGC
ENST00000697683.1:c.*1668_*1669delinsGC ENSP00000513395.1:n.*1668_*1669delinsGC
ENST00000697684.1:n.864_865delinsGC
ENST00000697685.1:c.*1501_*1502delinsGC ENSP00000513396.1:n.*1501_*1502delinsGC
ENST00000697686.1:c.453_454delinsGC ENSP00000513397.1:p.Met152Leu
ENST00000697687.1:n.683_684delinsGC
ENST00000697688.1:n.850_851delinsGC
ENST00000697689.1:c.*1340_*1341delinsGC ENSP00000513398.1:n.*1340_*1341delinsGC
ENST00000697690.1:c.804_805delinsGC ENSP00000513399.1:p.Met269Leu
ENST00000697691.1:c.*776_*777delinsGC ENSP00000513400.1:n.*776_*777delinsGC
ENST00000697692.1:c.*816_*817delinsGC ENSP00000513401.1:n.*816_*817delinsGC
ENST00000697694.1:c.453_454delinsGC ENSP00000513402.1:p.Met152Leu
ENST00000697695.1:n.1411_1412delinsGC
XM_006722001.2:c.804_805delinsGC XP_006722064.1:p.Met269Leu
XM_006722001.4:c.804_805delinsGC XP_006722064.1:p.Met269Leu
XM_006722002.2:c.804_805delinsGC XP_006722065.1:p.Met269Leu
XM_006722002.4:c.804_805delinsGC XP_006722065.1:p.Met269Leu
XM_006722004.2:c.453_454delinsGC XP_006722067.1:p.Met152Leu
XM_006722004.3:c.453_454delinsGC XP_006722067.1:p.Met152Leu
XM_006722005.2:c.453_454delinsGC XP_006722068.1:p.Met152Leu
XM_006722005.3:c.453_454delinsGC XP_006722068.1:p.Met152Leu
XM_011525092.1:c.453_454delinsGC XP_011523394.1:p.Met152Leu
XM_011525092.2:c.453_454delinsGC XP_011523394.1:p.Met152Leu
XM_011525093.1:c.453_454delinsGC XP_011523395.1:p.Met152Leu
XM_011525093.2:c.453_454delinsGC XP_011523395.1:p.Met152Leu
XM_011525094.1:c.453_454delinsGC XP_011523396.1:p.Met152Leu
XM_011525094.2:c.453_454delinsGC XP_011523396.1:p.Met152Leu
XM_017024914.1:c.453_454delinsGC XP_016880403.1:p.Met152Leu
XM_017024915.1:c.453_454delinsGC XP_016880404.1:p.Met152Leu
XM_017024916.1:c.453_454delinsGC XP_016880405.1:p.Met152Leu
XM_017024917.1:c.453_454delinsGC XP_016880406.1:p.Met152Leu
XM_017024918.2:c.453_454delinsGC XP_016880407.1:p.Met152Leu
XM_017024919.1:c.453_454delinsGC XP_016880408.1:p.Met152Leu
XR_934513.1:n.1022_1023delinsGC
XR_934513.3:n.1453_1454delinsGC
XR_934514.1:n.1022_1023delinsGC
XR_934514.3:n.1453_1454delinsGC