Canonical Allele Identifier: CA3261178708
Community Standard Title: NM_058216.3(RAD51C):c.710_711delinsAG (p.Arg237Gln)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709863_58709864delinsAG , CM000679.2:g.58709863_58709864delinsAG GRCh38
NC_000017.10:g.56787224_56787225delinsAG , CM000679.1:g.56787224_56787225delinsAG GRCh37
NC_000017.9:g.54142223_54142224delinsAG NCBI36
NG_023199.1:g.22262_22263delinsAG , LRG_314:g.22262_22263delinsAG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.710_711delinsAG MANE Select NP_478123.1:p.Arg237Gln
ENST00000337432.9:c.710_711delinsAG MANE Select ENSP00000336701.4:p.Arg237Gln
NM_058216.2:c.710_711delinsAG NP_478123.1:p.Arg237Gln
NR_103872.1:n.614_615delinsAG
NR_103872.2:n.585_586delinsAG
ENST00000337432.8:c.710_711delinsAG ENSP00000336701.4:p.Arg237Gln
ENST00000413590.5:c.348_349delinsAG
ENST00000425173.5:c.626_627delinsAG ENSP00000407282.1:p.Arg209Gln
ENST00000461271.5:c.359_360delinsAG ENSP00000464056.1:p.Arg120Gln
ENST00000461271.6:c.359_360delinsAG ENSP00000464056.2:p.Arg120Gln
ENST00000475762.5:c.*1413_*1414delinsAG ENSP00000432421.1:n.*1413_*1414delinsAG
ENST00000482007.5:c.*138_*139delinsAG ENSP00000433332.1:n.*138_*139delinsAG
ENST00000487525.5:c.*283_*284delinsAG ENSP00000431637.1:n.*283_*284delinsAG
ENST00000578151.1:n.45_46delinsAG
ENST00000581221.5:n.225_226delinsAG
ENST00000583539.5:c.710_711delinsAG ENSP00000463121.1:p.Arg237Gln
ENST00000584617.5:c.432_433delinsAG
ENST00000584804.1:c.5_6delinsAG ENSP00000463658.1:p.Arg2Gln
ENST00000697678.1:n.612_613delinsAG
ENST00000697679.1:n.1784_1785delinsAG
ENST00000697680.1:c.*1574_*1575delinsAG ENSP00000513392.1:n.*1574_*1575delinsAG
ENST00000697681.1:c.*1871_*1872delinsAG ENSP00000513393.1:n.*1871_*1872delinsAG
ENST00000697683.1:c.*1574_*1575delinsAG ENSP00000513395.1:n.*1574_*1575delinsAG
ENST00000697684.1:n.770_771delinsAG
ENST00000697685.1:c.*1407_*1408delinsAG ENSP00000513396.1:n.*1407_*1408delinsAG
ENST00000697686.1:c.359_360delinsAG ENSP00000513397.1:p.Arg120Gln
ENST00000697687.1:n.589_590delinsAG
ENST00000697688.1:n.756_757delinsAG
ENST00000697689.1:c.*1246_*1247delinsAG ENSP00000513398.1:n.*1246_*1247delinsAG
ENST00000697690.1:c.710_711delinsAG ENSP00000513399.1:p.Arg237Gln
ENST00000697691.1:c.*682_*683delinsAG ENSP00000513400.1:n.*682_*683delinsAG
ENST00000697692.1:c.*722_*723delinsAG ENSP00000513401.1:n.*722_*723delinsAG
ENST00000697694.1:c.359_360delinsAG ENSP00000513402.1:p.Arg120Gln
ENST00000697695.1:n.1317_1318delinsAG
XM_006722001.2:c.710_711delinsAG XP_006722064.1:p.Arg237Gln
XM_006722001.4:c.710_711delinsAG XP_006722064.1:p.Arg237Gln
XM_006722002.2:c.710_711delinsAG XP_006722065.1:p.Arg237Gln
XM_006722002.4:c.710_711delinsAG XP_006722065.1:p.Arg237Gln
XM_006722004.2:c.359_360delinsAG XP_006722067.1:p.Arg120Gln
XM_006722004.3:c.359_360delinsAG XP_006722067.1:p.Arg120Gln
XM_006722005.2:c.359_360delinsAG XP_006722068.1:p.Arg120Gln
XM_006722005.3:c.359_360delinsAG XP_006722068.1:p.Arg120Gln
XM_011525092.1:c.359_360delinsAG XP_011523394.1:p.Arg120Gln
XM_011525092.2:c.359_360delinsAG XP_011523394.1:p.Arg120Gln
XM_011525093.1:c.359_360delinsAG XP_011523395.1:p.Arg120Gln
XM_011525093.2:c.359_360delinsAG XP_011523395.1:p.Arg120Gln
XM_011525094.1:c.359_360delinsAG XP_011523396.1:p.Arg120Gln
XM_011525094.2:c.359_360delinsAG XP_011523396.1:p.Arg120Gln
XM_017024914.1:c.359_360delinsAG XP_016880403.1:p.Arg120Gln
XM_017024915.1:c.359_360delinsAG XP_016880404.1:p.Arg120Gln
XM_017024916.1:c.359_360delinsAG XP_016880405.1:p.Arg120Gln
XM_017024917.1:c.359_360delinsAG XP_016880406.1:p.Arg120Gln
XM_017024918.2:c.359_360delinsAG XP_016880407.1:p.Arg120Gln
XM_017024919.1:c.359_360delinsAG XP_016880408.1:p.Arg120Gln
XR_934513.1:n.928_929delinsAG
XR_934513.3:n.1359_1360delinsAG
XR_934514.1:n.928_929delinsAG
XR_934514.3:n.1359_1360delinsAG