Canonical Allele Identifier: CA400350018

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 2863056
• ClinVar RCV Id: RCV003617596
• dbSNP Id: rs2143801377
• MyVariant Identifiers: chr17:g.56780670T>A (hg19) ; chr17:g.58703309T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703309T>A , CM000679.2:g.58703309T>A	GRCh38
NC_000017.10:g.56780670T>A , CM000679.1:g.56780670T>A	GRCh37
NC_000017.9:g.54135669T>A	NCBI36
NG_023199.1:g.15708T>A , LRG_314:g.15708T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.334T>A	ENSP00000464056.2:p.Phe112Ile
ENST00000697677.1:n.1766T>A
ENST00000697678.1:n.587T>A
ENST00000697679.1:n.1759T>A
ENST00000697680.1:c.*1549T>A	ENSP00000513392.1:n.*1549T>A
ENST00000697681.1:c.*1701T>A	ENSP00000513393.1:n.*1701T>A
ENST00000697683.1:c.*1549T>A	ENSP00000513395.1:n.*1549T>A
ENST00000697684.1:n.745T>A
ENST00000697685.1:c.*1382T>A	ENSP00000513396.1:n.*1382T>A
ENST00000697686.1:c.334T>A	ENSP00000513397.1:p.Phe112Ile
ENST00000697687.1:n.564T>A
ENST00000697688.1:n.731T>A
ENST00000697689.1:c.*1221T>A	ENSP00000513398.1:n.*1221T>A
ENST00000697690.1:c.685T>A	ENSP00000513399.1:p.Phe229Ile
ENST00000697691.1:c.*657T>A	ENSP00000513400.1:n.*657T>A
ENST00000697692.1:c.*697T>A	ENSP00000513401.1:n.*697T>A
ENST00000697694.1:c.334T>A	ENSP00000513402.1:p.Phe112Ile
ENST00000697695.1:n.1292T>A
ENST00000337432.9:c.685T>A MANE Select	ENSP00000336701.4:p.Phe229Ile
ENST00000337432.8:c.685T>A	ENSP00000336701.4:p.Phe229Ile
ENST00000413590.5:c.323T>A
ENST00000425173.5:c.481T>A	ENSP00000407282.1:p.Phe161Ile
ENST00000461271.5:c.334T>A	ENSP00000464056.1:p.Phe112Ile
ENST00000475762.5:c.*1388T>A	ENSP00000432421.1:n.*1388T>A
ENST00000482007.5:c.*113T>A	ENSP00000433332.1:n.*113T>A
ENST00000487525.5:c.*113T>A	ENSP00000431637.1:n.*113T>A
ENST00000487921.5:n.597T>A
ENST00000583539.5:c.685T>A	ENSP00000463121.1:p.Phe229Ile
ENST00000584617.5:c.407T>A
NM_058216.2:c.685T>A	NP_478123.1:p.Phe229Ile
NR_103872.1:n.589T>A
XM_006722001.2:c.685T>A	XP_006722064.1:p.Phe229Ile
XM_006722002.2:c.685T>A	XP_006722065.1:p.Phe229Ile
XM_006722004.2:c.334T>A	XP_006722067.1:p.Phe112Ile
XM_006722005.2:c.334T>A	XP_006722068.1:p.Phe112Ile
XM_011525092.1:c.334T>A	XP_011523394.1:p.Phe112Ile
XM_011525093.1:c.334T>A	XP_011523395.1:p.Phe112Ile
XM_011525094.1:c.334T>A	XP_011523396.1:p.Phe112Ile
XR_934513.1:n.758T>A
XR_934514.1:n.758T>A
XM_006722001.4:c.685T>A	XP_006722064.1:p.Phe229Ile
XM_006722002.4:c.685T>A	XP_006722065.1:p.Phe229Ile
XM_006722004.3:c.334T>A	XP_006722067.1:p.Phe112Ile
XM_006722005.3:c.334T>A	XP_006722068.1:p.Phe112Ile
XM_011525092.2:c.334T>A	XP_011523394.1:p.Phe112Ile
XM_011525093.2:c.334T>A	XP_011523395.1:p.Phe112Ile
XM_011525094.2:c.334T>A	XP_011523396.1:p.Phe112Ile
XM_017024914.1:c.334T>A	XP_016880403.1:p.Phe112Ile
XM_017024915.1:c.334T>A	XP_016880404.1:p.Phe112Ile
XM_017024916.1:c.334T>A	XP_016880405.1:p.Phe112Ile
XM_017024917.1:c.334T>A	XP_016880406.1:p.Phe112Ile
XM_017024918.2:c.334T>A	XP_016880407.1:p.Phe112Ile
XM_017024919.1:c.334T>A	XP_016880408.1:p.Phe112Ile
XR_934513.3:n.1189T>A
XR_934514.3:n.1189T>A
NM_058216.3:c.685T>A MANE Select	NP_478123.1:p.Phe229Ile
NR_103872.2:n.560T>A