Canonical Allele Identifier: CA3261178809
Community Standard Title: NM_058216.3(RAD51C):c.988_989delinsAG (p.Pro330Ser)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732506_58732507delinsAG , CM000679.2:g.58732506_58732507delinsAG GRCh38
NC_000017.10:g.56809867_56809868delinsAG , CM000679.1:g.56809867_56809868delinsAG GRCh37
NC_000017.9:g.54164866_54164867delinsAG NCBI36
NG_023199.1:g.44905_44906delinsAG , LRG_314:g.44905_44906delinsAG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.988_989delinsAG MANE Select NP_478123.1:p.Pro330Ser
ENST00000337432.9:c.988_989delinsAG MANE Select ENSP00000336701.4:p.Pro330Ser
NM_058216.2:c.988_989delinsAG NP_478123.1:p.Pro330Ser
NR_103872.1:n.892_893delinsAG
NR_103872.2:n.863_864delinsAG
ENST00000337432.8:c.988_989delinsAG ENSP00000336701.4:p.Pro330Ser
ENST00000413590.5:c.629_630delinsAG
ENST00000461271.6:c.637_638delinsAG ENSP00000464056.2:p.Pro213Ser
ENST00000461706.1:n.175_176delinsAG
ENST00000475762.5:c.*1624_*1625delinsAG ENSP00000432421.1:n.*1624_*1625delinsAG
ENST00000482007.5:c.*416_*417delinsAG ENSP00000433332.1:n.*416_*417delinsAG
ENST00000487525.5:c.*564_*565delinsAG ENSP00000431637.1:n.*564_*565delinsAG
ENST00000578151.1:n.240-1612_240-1611delinsAG
ENST00000581221.5:n.503_504delinsAG
ENST00000583539.5:c.988_989delinsAG ENSP00000463121.1:p.Pro330Ser
ENST00000584617.5:c.710_711delinsAG
ENST00000584804.1:c.222_223delinsAG ENSP00000463658.1:p.His74_Pro75delinsGlnAla
ENST00000697680.1:c.*1952_*1953delinsAG ENSP00000513392.1:n.*1952_*1953delinsAG
ENST00000697681.1:c.*2149_*2150delinsAG ENSP00000513393.1:n.*2149_*2150delinsAG
ENST00000697683.1:c.*1924_*1925delinsAG ENSP00000513395.1:n.*1924_*1925delinsAG
ENST00000697685.1:c.*1685_*1686delinsAG ENSP00000513396.1:n.*1685_*1686delinsAG
ENST00000697686.1:c.759_760delinsAG ENSP00000513397.1:p.His253_Pro254delinsGlnAla
ENST00000697689.1:c.*1441-1612_*1441-1611delinsAG ENSP00000513398.1:n.*1441-1612_*1441-1611delinsAG
ENST00000697690.1:c.905-1612_905-1611delinsAG ENSP00000513399.1:n.905-1612_905-1611delinsAG
ENST00000697691.1:c.*960_*961delinsAG ENSP00000513400.1:n.*960_*961delinsAG
ENST00000697692.1:c.*1000_*1001delinsAG ENSP00000513401.1:n.*1000_*1001delinsAG
ENST00000697694.1:c.637_638delinsAG ENSP00000513402.1:p.Pro213Ser
ENST00000697695.1:n.1595_1596delinsAG
XM_006722001.2:c.991_992delinsAG XP_006722064.1:p.Pro331Ser
XM_006722001.4:c.991_992delinsAG XP_006722064.1:p.Pro331Ser
XM_006722002.2:c.927_928delinsAG XP_006722065.1:p.His309_Pro310delinsGlnAla
XM_006722002.4:c.927_928delinsAG XP_006722065.1:p.His309_Pro310delinsGlnAla
XM_006722004.2:c.640_641delinsAG XP_006722067.1:p.Pro214Ser
XM_006722004.3:c.640_641delinsAG XP_006722067.1:p.Pro214Ser
XM_006722005.2:c.640_641delinsAG XP_006722068.1:p.Pro214Ser
XM_006722005.3:c.640_641delinsAG XP_006722068.1:p.Pro214Ser
XM_011525092.1:c.640_641delinsAG XP_011523394.1:p.Pro214Ser
XM_011525092.2:c.640_641delinsAG XP_011523394.1:p.Pro214Ser
XM_011525093.1:c.640_641delinsAG XP_011523395.1:p.Pro214Ser
XM_011525093.2:c.640_641delinsAG XP_011523395.1:p.Pro214Ser
XM_011525094.1:c.640_641delinsAG XP_011523396.1:p.Pro214Ser
XM_011525094.2:c.640_641delinsAG XP_011523396.1:p.Pro214Ser
XM_017024914.1:c.637_638delinsAG XP_016880403.1:p.Pro213Ser
XM_017024915.1:c.637_638delinsAG XP_016880404.1:p.Pro213Ser
XM_017024916.1:c.637_638delinsAG XP_016880405.1:p.Pro213Ser
XM_017024917.1:c.637_638delinsAG XP_016880406.1:p.Pro213Ser
XM_017024918.2:c.637_638delinsAG XP_016880407.1:p.Pro213Ser
XM_017024919.1:c.576_577delinsAG XP_016880408.1:p.His192_Pro193delinsGlnAla
XR_934513.1:n.1206_1207delinsAG
XR_934513.3:n.1637_1638delinsAG
XR_934514.1:n.1209_1210delinsAG
XR_934514.3:n.1640_1641delinsAG
XR_934886.1:n.149+5564_149+5565delinsCT
XR_934886.2:n.149+5564_149+5565delinsCT