Canonical Allele Identifier: CA3261179022
Community Standard Title: NM_058216.3(RAD51C):c.998_999delinsTC (p.Lys333Ile)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732516_58732517delinsTC , CM000679.2:g.58732516_58732517delinsTC GRCh38
NC_000017.10:g.56809877_56809878delinsTC , CM000679.1:g.56809877_56809878delinsTC GRCh37
NC_000017.9:g.54164876_54164877delinsTC NCBI36
NG_023199.1:g.44915_44916delinsTC , LRG_314:g.44915_44916delinsTC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.998_999delinsTC MANE Select NP_478123.1:p.Lys333Ile
ENST00000337432.9:c.998_999delinsTC MANE Select ENSP00000336701.4:p.Lys333Ile
NM_058216.2:c.998_999delinsTC NP_478123.1:p.Lys333Ile
NR_103872.1:n.902_903delinsTC
NR_103872.2:n.873_874delinsTC
ENST00000337432.8:c.998_999delinsTC ENSP00000336701.4:p.Lys333Ile
ENST00000413590.5:c.639_640delinsTC
ENST00000461271.6:c.647_648delinsTC ENSP00000464056.2:p.Lys216Ile
ENST00000461706.1:n.185_186delinsTC
ENST00000475762.5:c.*1634_*1635delinsTC ENSP00000432421.1:n.*1634_*1635delinsTC
ENST00000482007.5:c.*426_*427delinsTC ENSP00000433332.1:n.*426_*427delinsTC
ENST00000487525.5:c.*574_*575delinsTC ENSP00000431637.1:n.*574_*575delinsTC
ENST00000578151.1:n.240-1602_240-1601delinsTC
ENST00000581221.5:n.513_514delinsTC
ENST00000583539.5:c.998_999delinsTC ENSP00000463121.1:p.Lys333Ile
ENST00000584617.5:c.720_721delinsTC
ENST00000584804.1:c.232_233delinsTC ENSP00000463658.1:p.Arg78Ser
ENST00000697680.1:c.*1962_*1963delinsTC ENSP00000513392.1:n.*1962_*1963delinsTC
ENST00000697681.1:c.*2159_*2160delinsTC ENSP00000513393.1:n.*2159_*2160delinsTC
ENST00000697683.1:c.*1934_*1935delinsTC ENSP00000513395.1:n.*1934_*1935delinsTC
ENST00000697685.1:c.*1695_*1696delinsTC ENSP00000513396.1:n.*1695_*1696delinsTC
ENST00000697686.1:c.769_770delinsTC ENSP00000513397.1:p.Arg257Ser
ENST00000697689.1:c.*1441-1602_*1441-1601delinsTC ENSP00000513398.1:n.*1441-1602_*1441-1601delinsTC
ENST00000697690.1:c.905-1602_905-1601delinsTC ENSP00000513399.1:n.905-1602_905-1601delinsTC
ENST00000697691.1:c.*970_*971delinsTC ENSP00000513400.1:n.*970_*971delinsTC
ENST00000697692.1:c.*1010_*1011delinsTC ENSP00000513401.1:n.*1010_*1011delinsTC
ENST00000697694.1:c.647_648delinsTC ENSP00000513402.1:p.Lys216Ile
ENST00000697695.1:n.1605_1606delinsTC
XM_006722001.2:c.1001_1002delinsTC XP_006722064.1:p.Lys334Ile
XM_006722001.4:c.1001_1002delinsTC XP_006722064.1:p.Lys334Ile
XM_006722002.2:c.937_938delinsTC XP_006722065.1:p.Arg313Ser
XM_006722002.4:c.937_938delinsTC XP_006722065.1:p.Arg313Ser
XM_006722004.2:c.650_651delinsTC XP_006722067.1:p.Lys217Ile
XM_006722004.3:c.650_651delinsTC XP_006722067.1:p.Lys217Ile
XM_006722005.2:c.650_651delinsTC XP_006722068.1:p.Lys217Ile
XM_006722005.3:c.650_651delinsTC XP_006722068.1:p.Lys217Ile
XM_011525092.1:c.650_651delinsTC XP_011523394.1:p.Lys217Ile
XM_011525092.2:c.650_651delinsTC XP_011523394.1:p.Lys217Ile
XM_011525093.1:c.650_651delinsTC XP_011523395.1:p.Lys217Ile
XM_011525093.2:c.650_651delinsTC XP_011523395.1:p.Lys217Ile
XM_011525094.1:c.650_651delinsTC XP_011523396.1:p.Lys217Ile
XM_011525094.2:c.650_651delinsTC XP_011523396.1:p.Lys217Ile
XM_017024914.1:c.647_648delinsTC XP_016880403.1:p.Lys216Ile
XM_017024915.1:c.647_648delinsTC XP_016880404.1:p.Lys216Ile
XM_017024916.1:c.647_648delinsTC XP_016880405.1:p.Lys216Ile
XM_017024917.1:c.647_648delinsTC XP_016880406.1:p.Lys216Ile
XM_017024918.2:c.647_648delinsTC XP_016880407.1:p.Lys216Ile
XM_017024919.1:c.586_587delinsTC XP_016880408.1:p.Arg196Ser
XR_934513.1:n.1216_1217delinsTC
XR_934513.3:n.1647_1648delinsTC
XR_934514.1:n.1219_1220delinsTC
XR_934514.3:n.1650_1651delinsTC
XR_934886.1:n.149+5554_149+5555delinsGA
XR_934886.2:n.149+5554_149+5555delinsGA