Canonical Allele Identifier: CA3057242524
Community Standard Title: NM_058216.3(RAD51C):c.645_647delinsTTG (p.Tyr216Cys)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703269_58703271delinsTTG , CM000679.2:g.58703269_58703271delinsTTG GRCh38
NC_000017.10:g.56780630_56780632delinsTTG , CM000679.1:g.56780630_56780632delinsTTG GRCh37
NC_000017.9:g.54135629_54135631delinsTTG NCBI36
NG_023199.1:g.15668_15670delinsTTG , LRG_314:g.15668_15670delinsTTG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.645_647delinsTTG MANE Select NP_478123.1:p.Tyr216Cys
ENST00000337432.9:c.645_647delinsTTG MANE Select ENSP00000336701.4:p.Tyr216Cys
NM_058216.2:c.645_647delinsTTG NP_478123.1:p.Tyr216Cys
NR_103872.1:n.549_551delinsTTG
NR_103872.2:n.520_522delinsTTG
ENST00000337432.8:c.645_647delinsTTG ENSP00000336701.4:p.Tyr216Cys
ENST00000413590.5:c.283_285delinsTTG
ENST00000425173.5:c.441_443delinsTTG ENSP00000407282.1:p.Tyr148Cys
ENST00000461271.5:c.294_296delinsTTG ENSP00000464056.1:p.Tyr99Cys
ENST00000461271.6:c.294_296delinsTTG ENSP00000464056.2:p.Tyr99Cys
ENST00000475762.5:c.*1348_*1350delinsTTG ENSP00000432421.1:n.*1348_*1350delinsTTG
ENST00000482007.5:c.*73_*75delinsTTG ENSP00000433332.1:n.*73_*75delinsTTG
ENST00000487525.5:c.*73_*75delinsTTG ENSP00000431637.1:n.*73_*75delinsTTG
ENST00000487921.5:n.557_559delinsTTG
ENST00000583539.5:c.645_647delinsTTG ENSP00000463121.1:p.Tyr216Cys
ENST00000584617.5:c.367_369delinsTTG
ENST00000697677.1:n.1726_1728delinsTTG
ENST00000697678.1:n.547_549delinsTTG
ENST00000697679.1:n.1719_1721delinsTTG
ENST00000697680.1:c.*1509_*1511delinsTTG ENSP00000513392.1:n.*1509_*1511delinsTTG
ENST00000697681.1:c.*1661_*1663delinsTTG ENSP00000513393.1:n.*1661_*1663delinsTTG
ENST00000697683.1:c.*1509_*1511delinsTTG ENSP00000513395.1:n.*1509_*1511delinsTTG
ENST00000697684.1:n.705_707delinsTTG
ENST00000697685.1:c.*1342_*1344delinsTTG ENSP00000513396.1:n.*1342_*1344delinsTTG
ENST00000697686.1:c.294_296delinsTTG ENSP00000513397.1:p.Tyr99Cys
ENST00000697687.1:n.524_526delinsTTG
ENST00000697688.1:n.691_693delinsTTG
ENST00000697689.1:c.*1181_*1183delinsTTG ENSP00000513398.1:n.*1181_*1183delinsTTG
ENST00000697690.1:c.645_647delinsTTG ENSP00000513399.1:p.Tyr216Cys
ENST00000697691.1:c.*617_*619delinsTTG ENSP00000513400.1:n.*617_*619delinsTTG
ENST00000697692.1:c.*657_*659delinsTTG ENSP00000513401.1:n.*657_*659delinsTTG
ENST00000697694.1:c.294_296delinsTTG ENSP00000513402.1:p.Tyr99Cys
ENST00000697695.1:n.1252_1254delinsTTG
XM_006722001.2:c.645_647delinsTTG XP_006722064.1:p.Tyr216Cys
XM_006722001.4:c.645_647delinsTTG XP_006722064.1:p.Tyr216Cys
XM_006722002.2:c.645_647delinsTTG XP_006722065.1:p.Tyr216Cys
XM_006722002.4:c.645_647delinsTTG XP_006722065.1:p.Tyr216Cys
XM_006722004.2:c.294_296delinsTTG XP_006722067.1:p.Tyr99Cys
XM_006722004.3:c.294_296delinsTTG XP_006722067.1:p.Tyr99Cys
XM_006722005.2:c.294_296delinsTTG XP_006722068.1:p.Tyr99Cys
XM_006722005.3:c.294_296delinsTTG XP_006722068.1:p.Tyr99Cys
XM_011525092.1:c.294_296delinsTTG XP_011523394.1:p.Tyr99Cys
XM_011525092.2:c.294_296delinsTTG XP_011523394.1:p.Tyr99Cys
XM_011525093.1:c.294_296delinsTTG XP_011523395.1:p.Tyr99Cys
XM_011525093.2:c.294_296delinsTTG XP_011523395.1:p.Tyr99Cys
XM_011525094.1:c.294_296delinsTTG XP_011523396.1:p.Tyr99Cys
XM_011525094.2:c.294_296delinsTTG XP_011523396.1:p.Tyr99Cys
XM_017024914.1:c.294_296delinsTTG XP_016880403.1:p.Tyr99Cys
XM_017024915.1:c.294_296delinsTTG XP_016880404.1:p.Tyr99Cys
XM_017024916.1:c.294_296delinsTTG XP_016880405.1:p.Tyr99Cys
XM_017024917.1:c.294_296delinsTTG XP_016880406.1:p.Tyr99Cys
XM_017024918.2:c.294_296delinsTTG XP_016880407.1:p.Tyr99Cys
XM_017024919.1:c.294_296delinsTTG XP_016880408.1:p.Tyr99Cys
XR_934513.1:n.718_720delinsTTG
XR_934513.3:n.1149_1151delinsTTG
XR_934514.1:n.718_720delinsTTG
XR_934514.3:n.1149_1151delinsTTG