Canonical Allele Identifier: CA8677379

Gene: RAD51C

Linked Data

• dbSNP Id: rs758794484
• ExAC: 17:56809827 TTC / T
• gnomAD v2: 17-56809827-TTC-T
• MyVariant Identifiers: chr17:g.56809828_56809829del (hg19) ; chr17:g.58732468_58732469del (hg38) ; chr17:g.58732467_58732468del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58732468_58732469del , CM000679.2:g.58732468_58732469del	GRCh38
NC_000017.10:g.56809829_56809830del , CM000679.1:g.56809829_56809830del	GRCh37
NC_000017.9:g.54164828_54164829del	NCBI36
NG_023199.1:g.44867_44868del , LRG_314:g.44867_44868del

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.615-16_615-15del	ENSP00000464056.2:n.615-16_615-15del
ENST00000697680.1:c.*1930-16_*1930-15del	ENSP00000513392.1:n.*1930-16_*1930-15del
ENST00000697681.1:c.*2127-16_*2127-15del	ENSP00000513393.1:n.*2127-16_*2127-15del
ENST00000697683.1:c.*1902-16_*1902-15del	ENSP00000513395.1:n.*1902-16_*1902-15del
ENST00000697685.1:c.*1663-16_*1663-15del	ENSP00000513396.1:n.*1663-16_*1663-15del
ENST00000697686.1:c.737-16_737-15del	ENSP00000513397.1:n.737-16_737-15del
ENST00000697689.1:c.*1441-1650_*1441-1649del	ENSP00000513398.1:n.*1441-1650_*1441-1649...
ENST00000697690.1:c.905-1650_905-1649del	ENSP00000513399.1:n.905-1650_905-1649del
ENST00000697691.1:c.*938-16_*938-15del	ENSP00000513400.1:n.*938-16_*938-15del
ENST00000697692.1:c.*978-16_*978-15del	ENSP00000513401.1:n.*978-16_*978-15del
ENST00000697694.1:c.615-16_615-15del	ENSP00000513402.1:n.615-16_615-15del
ENST00000697695.1:n.1573-16_1573-15del
ENST00000337432.9:c.966-16_966-15del MANE Select	ENSP00000336701.4:n.966-16_966-15del
ENST00000337432.8:c.966-16_966-15del	ENSP00000336701.4:n.966-16_966-15del
ENST00000413590.5:c.604-13_604-12del
ENST00000461706.1:n.137_138del
ENST00000475762.5:c.*1602-16_*1602-15del	ENSP00000432421.1:n.*1602-16_*1602-15del
ENST00000482007.5:c.*394-16_*394-15del	ENSP00000433332.1:n.*394-16_*394-15del
ENST00000487525.5:c.*539-13_*539-12del	ENSP00000431637.1:n.*539-13_*539-12del
ENST00000578151.1:n.240-1650_240-1649del
ENST00000581221.5:n.481-16_481-15del
ENST00000583539.5:c.966-16_966-15del	ENSP00000463121.1:n.966-16_966-15del
ENST00000584617.5:c.688-16_688-15del
ENST00000584804.1:c.200-16_200-15del	ENSP00000463658.1:n.200-16_200-15del
NM_058216.2:c.966-16_966-15del	NP_478123.1:n.966-16_966-15del
NR_103872.1:n.870-16_870-15del
XM_006722001.2:c.966-13_966-12del	XP_006722064.1:n.966-13_966-12del
XM_006722002.2:c.905-16_905-15del	XP_006722065.1:n.905-16_905-15del
XM_006722004.2:c.615-13_615-12del	XP_006722067.1:n.615-13_615-12del
XM_006722005.2:c.615-13_615-12del	XP_006722068.1:n.615-13_615-12del
XM_011525092.1:c.615-13_615-12del	XP_011523394.1:n.615-13_615-12del
XM_011525093.1:c.615-13_615-12del	XP_011523395.1:n.615-13_615-12del
XM_011525094.1:c.615-13_615-12del	XP_011523396.1:n.615-13_615-12del
XR_934513.1:n.1184-16_1184-15del
XR_934514.1:n.1184-13_1184-12del
XR_934886.1:n.149+5603_149+5604del
XM_006722001.4:c.966-13_966-12del	XP_006722064.1:n.966-13_966-12del
XM_006722002.4:c.905-16_905-15del	XP_006722065.1:n.905-16_905-15del
XM_006722004.3:c.615-13_615-12del	XP_006722067.1:n.615-13_615-12del
XM_006722005.3:c.615-13_615-12del	XP_006722068.1:n.615-13_615-12del
XM_011525092.2:c.615-13_615-12del	XP_011523394.1:n.615-13_615-12del
XM_011525093.2:c.615-13_615-12del	XP_011523395.1:n.615-13_615-12del
XM_011525094.2:c.615-13_615-12del	XP_011523396.1:n.615-13_615-12del
XM_017024914.1:c.615-16_615-15del	XP_016880403.1:n.615-16_615-15del
XM_017024915.1:c.615-16_615-15del	XP_016880404.1:n.615-16_615-15del
XM_017024916.1:c.615-16_615-15del	XP_016880405.1:n.615-16_615-15del
XM_017024917.1:c.615-16_615-15del	XP_016880406.1:n.615-16_615-15del
XM_017024918.2:c.615-16_615-15del	XP_016880407.1:n.615-16_615-15del
XM_017024919.1:c.554-16_554-15del	XP_016880408.1:n.554-16_554-15del
XR_934513.3:n.1615-16_1615-15del
XR_934514.3:n.1615-13_1615-12del
XR_934886.2:n.149+5603_149+5604del
NM_058216.3:c.966-16_966-15del MANE Select	NP_478123.1:n.966-16_966-15del
NR_103872.2:n.841-16_841-15del