Canonical Allele Identifier: CA400349158

Gene: RAD51C

Linked Data

• dbSNP Id: rs2143797075
• gnomAD v4: 17-58703216-G-A
• MyVariant Identifiers: chr17:g.56780577G>A (hg19) ; chr17:g.58703216G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703216G>A , CM000679.2:g.58703216G>A	GRCh38
NC_000017.10:g.56780577G>A , CM000679.1:g.56780577G>A	GRCh37
NC_000017.9:g.54135576G>A	NCBI36
NG_023199.1:g.15615G>A , LRG_314:g.15615G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.241G>A	ENSP00000464056.2:p.Asp81Asn
ENST00000697677.1:n.1673G>A
ENST00000697678.1:n.494G>A
ENST00000697679.1:n.1666G>A
ENST00000697680.1:c.*1456G>A	ENSP00000513392.1:n.*1456G>A
ENST00000697681.1:c.*1608G>A	ENSP00000513393.1:n.*1608G>A
ENST00000697683.1:c.*1456G>A	ENSP00000513395.1:n.*1456G>A
ENST00000697684.1:n.652G>A
ENST00000697685.1:c.*1289G>A	ENSP00000513396.1:n.*1289G>A
ENST00000697686.1:c.241G>A	ENSP00000513397.1:p.Asp81Asn
ENST00000697687.1:n.471G>A
ENST00000697688.1:n.638G>A
ENST00000697689.1:c.*1128G>A	ENSP00000513398.1:n.*1128G>A
ENST00000697690.1:c.592G>A	ENSP00000513399.1:p.Asp198Asn
ENST00000697691.1:c.*564G>A	ENSP00000513400.1:n.*564G>A
ENST00000697692.1:c.*604G>A	ENSP00000513401.1:n.*604G>A
ENST00000697694.1:c.241G>A	ENSP00000513402.1:p.Asp81Asn
ENST00000697695.1:n.1199G>A
ENST00000337432.9:c.592G>A MANE Select	ENSP00000336701.4:p.Asp198Asn
ENST00000337432.8:c.592G>A	ENSP00000336701.4:p.Asp198Asn
ENST00000413590.5:c.230G>A
ENST00000425173.5:c.388G>A	ENSP00000407282.1:p.Asp130Asn
ENST00000461271.5:c.241G>A	ENSP00000464056.1:p.Asp81Asn
ENST00000475762.5:c.*1295G>A	ENSP00000432421.1:n.*1295G>A
ENST00000482007.5:c.*20G>A	ENSP00000433332.1:n.*20G>A
ENST00000487525.5:c.*20G>A	ENSP00000431637.1:n.*20G>A
ENST00000487921.5:n.504G>A
ENST00000583539.5:c.592G>A	ENSP00000463121.1:p.Asp198Asn
ENST00000584617.5:c.314G>A
NM_058216.2:c.592G>A	NP_478123.1:p.Asp198Asn
NR_103872.1:n.496G>A
XM_006722001.2:c.592G>A	XP_006722064.1:p.Asp198Asn
XM_006722002.2:c.592G>A	XP_006722065.1:p.Asp198Asn
XM_006722004.2:c.241G>A	XP_006722067.1:p.Asp81Asn
XM_006722005.2:c.241G>A	XP_006722068.1:p.Asp81Asn
XM_011525092.1:c.241G>A	XP_011523394.1:p.Asp81Asn
XM_011525093.1:c.241G>A	XP_011523395.1:p.Asp81Asn
XM_011525094.1:c.241G>A	XP_011523396.1:p.Asp81Asn
XR_934513.1:n.665G>A
XR_934514.1:n.665G>A
XM_006722001.4:c.592G>A	XP_006722064.1:p.Asp198Asn
XM_006722002.4:c.592G>A	XP_006722065.1:p.Asp198Asn
XM_006722004.3:c.241G>A	XP_006722067.1:p.Asp81Asn
XM_006722005.3:c.241G>A	XP_006722068.1:p.Asp81Asn
XM_011525092.2:c.241G>A	XP_011523394.1:p.Asp81Asn
XM_011525093.2:c.241G>A	XP_011523395.1:p.Asp81Asn
XM_011525094.2:c.241G>A	XP_011523396.1:p.Asp81Asn
XM_017024914.1:c.241G>A	XP_016880403.1:p.Asp81Asn
XM_017024915.1:c.241G>A	XP_016880404.1:p.Asp81Asn
XM_017024916.1:c.241G>A	XP_016880405.1:p.Asp81Asn
XM_017024917.1:c.241G>A	XP_016880406.1:p.Asp81Asn
XM_017024918.2:c.241G>A	XP_016880407.1:p.Asp81Asn
XM_017024919.1:c.241G>A	XP_016880408.1:p.Asp81Asn
XR_934513.3:n.1096G>A
XR_934514.3:n.1096G>A
NM_058216.3:c.592G>A MANE Select	NP_478123.1:p.Asp198Asn
NR_103872.2:n.467G>A