Canonical Allele Identifier: CA985031704

Gene: RAD51C

Linked Data

• dbSNP Id: rs2048488189
• gnomAD v3: 17-58709720-T-TAA
• gnomAD v4: 17-58709720-T-TAA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709720_58709721insAA , CM000679.2:g.58709720_58709721insAA	GRCh38
NC_000017.10:g.56787081_56787082insAA , CM000679.1:g.56787081_56787082insAA	GRCh37
NC_000017.9:g.54142080_54142081insAA	NCBI36
NG_023199.1:g.22119_22120insAA , LRG_314:g.22119_22120insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.355-139_355-138insAA	ENSP00000464056.2:n.355-139_355-138insAA
ENST00000697678.1:n.608-139_608-138insAA
ENST00000697679.1:n.1780-139_1780-138insAA
ENST00000697680.1:c.*1570-139_*1570-138insAA	ENSP00000513392.1:n.*1570-139_*1570-138insAA
ENST00000697681.1:c.*1867-139_*1867-138insAA	ENSP00000513393.1:n.*1867-139_*1867-138insAA
ENST00000697683.1:c.*1570-139_*1570-138insAA	ENSP00000513395.1:n.*1570-139_*1570-138insAA
ENST00000697684.1:n.766-139_766-138insAA
ENST00000697685.1:c.*1403-139_*1403-138insAA	ENSP00000513396.1:n.*1403-139_*1403-138insAA
ENST00000697686.1:c.355-139_355-138insAA	ENSP00000513397.1:n.355-139_355-138insAA
ENST00000697687.1:n.585-139_585-138insAA
ENST00000697688.1:n.752-139_752-138insAA
ENST00000697689.1:c.*1242-139_*1242-138insAA	ENSP00000513398.1:n.*1242-139_*1242-138insAA
ENST00000697690.1:c.706-139_706-138insAA	ENSP00000513399.1:n.706-139_706-138insAA
ENST00000697691.1:c.*678-139_*678-138insAA	ENSP00000513400.1:n.*678-139_*678-138insAA
ENST00000697692.1:c.*718-139_*718-138insAA	ENSP00000513401.1:n.*718-139_*718-138insAA
ENST00000697694.1:c.355-139_355-138insAA	ENSP00000513402.1:n.355-139_355-138insAA
ENST00000697695.1:n.1313-139_1313-138insAA
ENST00000337432.9:c.706-139_706-138insAA MANE Select	ENSP00000336701.4:n.706-139_706-138insAA
ENST00000337432.8:c.706-139_706-138insAA	ENSP00000336701.4:n.706-139_706-138insAA
ENST00000413590.5:c.344-139_344-138insAA
ENST00000425173.5:c.622-139_622-138insAA	ENSP00000407282.1:n.622-139_622-138insAA
ENST00000461271.5:c.355-139_355-138insAA	ENSP00000464056.1:n.355-139_355-138insAA
ENST00000475762.5:c.*1409-139_*1409-138insAA	ENSP00000432421.1:n.*1409-139_*1409-138insAA
ENST00000482007.5:c.*134-139_*134-138insAA	ENSP00000433332.1:n.*134-139_*134-138insAA
ENST00000487525.5:c.*279-139_*279-138insAA	ENSP00000431637.1:n.*279-139_*279-138insAA
ENST00000581221.5:n.82_83insAA
ENST00000583539.5:c.706-139_706-138insAA	ENSP00000463121.1:n.706-139_706-138insAA
ENST00000584617.5:c.428-139_428-138insAA
NM_058216.2:c.706-139_706-138insAA	NP_478123.1:n.706-139_706-138insAA
NR_103872.1:n.610-139_610-138insAA
XM_006722001.2:c.706-139_706-138insAA	XP_006722064.1:n.706-139_706-138insAA
XM_006722002.2:c.706-139_706-138insAA	XP_006722065.1:n.706-139_706-138insAA
XM_006722004.2:c.355-139_355-138insAA	XP_006722067.1:n.355-139_355-138insAA
XM_006722005.2:c.355-139_355-138insAA	XP_006722068.1:n.355-139_355-138insAA
XM_011525092.1:c.355-139_355-138insAA	XP_011523394.1:n.355-139_355-138insAA
XM_011525093.1:c.355-139_355-138insAA	XP_011523395.1:n.355-139_355-138insAA
XM_011525094.1:c.355-139_355-138insAA	XP_011523396.1:n.355-139_355-138insAA
XR_934513.1:n.924-139_924-138insAA
XR_934514.1:n.924-139_924-138insAA
XM_006722001.4:c.706-139_706-138insAA	XP_006722064.1:n.706-139_706-138insAA
XM_006722002.4:c.706-139_706-138insAA	XP_006722065.1:n.706-139_706-138insAA
XM_006722004.3:c.355-139_355-138insAA	XP_006722067.1:n.355-139_355-138insAA
XM_006722005.3:c.355-139_355-138insAA	XP_006722068.1:n.355-139_355-138insAA
XM_011525092.2:c.355-139_355-138insAA	XP_011523394.1:n.355-139_355-138insAA
XM_011525093.2:c.355-139_355-138insAA	XP_011523395.1:n.355-139_355-138insAA
XM_011525094.2:c.355-139_355-138insAA	XP_011523396.1:n.355-139_355-138insAA
XM_017024914.1:c.355-139_355-138insAA	XP_016880403.1:n.355-139_355-138insAA
XM_017024915.1:c.355-139_355-138insAA	XP_016880404.1:n.355-139_355-138insAA
XM_017024916.1:c.355-139_355-138insAA	XP_016880405.1:n.355-139_355-138insAA
XM_017024917.1:c.355-139_355-138insAA	XP_016880406.1:n.355-139_355-138insAA
XM_017024918.2:c.355-139_355-138insAA	XP_016880407.1:n.355-139_355-138insAA
XM_017024919.1:c.355-139_355-138insAA	XP_016880408.1:n.355-139_355-138insAA
XR_934513.3:n.1355-139_1355-138insAA
XR_934514.3:n.1355-139_1355-138insAA
NM_058216.3:c.706-139_706-138insAA MANE Select	NP_478123.1:n.706-139_706-138insAA
NR_103872.2:n.581-139_581-138insAA