Canonical Allele Identifier: CA2639017080

Gene: RAD51C

Linked Data

• gnomAD v4: 17-58732361-TAGAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58732363_58732366del , CM000679.2:g.58732363_58732366del	GRCh38
NC_000017.10:g.56809724_56809727del , CM000679.1:g.56809724_56809727del	GRCh37
NC_000017.9:g.54164723_54164726del	NCBI36
NG_023199.1:g.44762_44765del , LRG_314:g.44762_44765del

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.615-121_615-118del	ENSP00000464056.2:n.615-121_615-118del
ENST00000697680.1:c.*1930-121_*1930-118del	ENSP00000513392.1:n.*1930-121_*1930-118del
ENST00000697681.1:c.*2127-121_*2127-118del	ENSP00000513393.1:n.*2127-121_*2127-118del
ENST00000697683.1:c.*1902-121_*1902-118del	ENSP00000513395.1:n.*1902-121_*1902-118del
ENST00000697685.1:c.*1663-121_*1663-118del	ENSP00000513396.1:n.*1663-121_*1663-118del
ENST00000697686.1:c.737-121_737-118del	ENSP00000513397.1:n.737-121_737-118del
ENST00000697689.1:c.*1441-1755_*1441-1752del	ENSP00000513398.1:n.*1441-1755_*1441-1752del
ENST00000697690.1:c.905-1755_905-1752del	ENSP00000513399.1:n.905-1755_905-1752del
ENST00000697691.1:c.*938-121_*938-118del	ENSP00000513400.1:n.*938-121_*938-118del
ENST00000697692.1:c.*978-121_*978-118del	ENSP00000513401.1:n.*978-121_*978-118del
ENST00000697694.1:c.615-121_615-118del	ENSP00000513402.1:n.615-121_615-118del
ENST00000697695.1:n.1573-121_1573-118del
ENST00000337432.9:c.966-121_966-118del MANE Select	ENSP00000336701.4:n.966-121_966-118del
ENST00000337432.8:c.966-121_966-118del	ENSP00000336701.4:n.966-121_966-118del
ENST00000413590.5:c.604-118_604-115del
ENST00000461706.1:n.32_35del
ENST00000475762.5:c.*1602-121_*1602-118del	ENSP00000432421.1:n.*1602-121_*1602-118del
ENST00000482007.5:c.*394-121_*394-118del	ENSP00000433332.1:n.*394-121_*394-118del
ENST00000487525.5:c.*539-118_*539-115del	ENSP00000431637.1:n.*539-118_*539-115del
ENST00000578151.1:n.240-1755_240-1752del
ENST00000581221.5:n.481-121_481-118del
ENST00000583539.5:c.966-121_966-118del	ENSP00000463121.1:n.966-121_966-118del
ENST00000584617.5:c.688-121_688-118del
ENST00000584804.1:c.200-121_200-118del	ENSP00000463658.1:n.200-121_200-118del
NM_058216.2:c.966-121_966-118del	NP_478123.1:n.966-121_966-118del
NR_103872.1:n.870-121_870-118del
XM_006722001.2:c.966-118_966-115del	XP_006722064.1:n.966-118_966-115del
XM_006722002.2:c.905-121_905-118del	XP_006722065.1:n.905-121_905-118del
XM_006722004.2:c.615-118_615-115del	XP_006722067.1:n.615-118_615-115del
XM_006722005.2:c.615-118_615-115del	XP_006722068.1:n.615-118_615-115del
XM_011525092.1:c.615-118_615-115del	XP_011523394.1:n.615-118_615-115del
XM_011525093.1:c.615-118_615-115del	XP_011523395.1:n.615-118_615-115del
XM_011525094.1:c.615-118_615-115del	XP_011523396.1:n.615-118_615-115del
XR_934513.1:n.1184-121_1184-118del
XR_934514.1:n.1184-118_1184-115del
XR_934886.1:n.149+5706_149+5709del
XM_006722001.4:c.966-118_966-115del	XP_006722064.1:n.966-118_966-115del
XM_006722002.4:c.905-121_905-118del	XP_006722065.1:n.905-121_905-118del
XM_006722004.3:c.615-118_615-115del	XP_006722067.1:n.615-118_615-115del
XM_006722005.3:c.615-118_615-115del	XP_006722068.1:n.615-118_615-115del
XM_011525092.2:c.615-118_615-115del	XP_011523394.1:n.615-118_615-115del
XM_011525093.2:c.615-118_615-115del	XP_011523395.1:n.615-118_615-115del
XM_011525094.2:c.615-118_615-115del	XP_011523396.1:n.615-118_615-115del
XM_017024914.1:c.615-121_615-118del	XP_016880403.1:n.615-121_615-118del
XM_017024915.1:c.615-121_615-118del	XP_016880404.1:n.615-121_615-118del
XM_017024916.1:c.615-121_615-118del	XP_016880405.1:n.615-121_615-118del
XM_017024917.1:c.615-121_615-118del	XP_016880406.1:n.615-121_615-118del
XM_017024918.2:c.615-121_615-118del	XP_016880407.1:n.615-121_615-118del
XM_017024919.1:c.554-121_554-118del	XP_016880408.1:n.554-121_554-118del
XR_934513.3:n.1615-121_1615-118del
XR_934514.3:n.1615-118_1615-115del
XR_934886.2:n.149+5706_149+5709del
NM_058216.3:c.966-121_966-118del MANE Select	NP_478123.1:n.966-121_966-118del
NR_103872.2:n.841-121_841-118del