Canonical Allele Identifier: CA400353394

Gene: RAD51C

Linked Data

• dbSNP Id: rs1431468155
• MyVariant Identifiers: chr17:g.56787247G>C (hg19) ; chr17:g.58709886G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709886G>C , CM000679.2:g.58709886G>C	GRCh38
NC_000017.10:g.56787247G>C , CM000679.1:g.56787247G>C	GRCh37
NC_000017.9:g.54142246G>C	NCBI36
NG_023199.1:g.22285G>C , LRG_314:g.22285G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.382G>C	ENSP00000464056.2:p.Ala128Pro
ENST00000697678.1:n.635G>C
ENST00000697679.1:n.1807G>C
ENST00000697680.1:c.*1597G>C	ENSP00000513392.1:n.*1597G>C
ENST00000697681.1:c.*1894G>C	ENSP00000513393.1:n.*1894G>C
ENST00000697683.1:c.*1597G>C	ENSP00000513395.1:n.*1597G>C
ENST00000697684.1:n.793G>C
ENST00000697685.1:c.*1430G>C	ENSP00000513396.1:n.*1430G>C
ENST00000697686.1:c.382G>C	ENSP00000513397.1:p.Ala128Pro
ENST00000697687.1:n.612G>C
ENST00000697688.1:n.779G>C
ENST00000697689.1:c.*1269G>C	ENSP00000513398.1:n.*1269G>C
ENST00000697690.1:c.733G>C	ENSP00000513399.1:p.Ala245Pro
ENST00000697691.1:c.*705G>C	ENSP00000513400.1:n.*705G>C
ENST00000697692.1:c.*745G>C	ENSP00000513401.1:n.*745G>C
ENST00000697694.1:c.382G>C	ENSP00000513402.1:p.Ala128Pro
ENST00000697695.1:n.1340G>C
ENST00000337432.9:c.733G>C MANE Select	ENSP00000336701.4:p.Ala245Pro
ENST00000337432.8:c.733G>C	ENSP00000336701.4:p.Ala245Pro
ENST00000413590.5:c.371G>C
ENST00000461271.5:c.382G>C	ENSP00000464056.1:p.Ala128Pro
ENST00000475762.5:c.*1436G>C	ENSP00000432421.1:n.*1436G>C
ENST00000482007.5:c.*161G>C	ENSP00000433332.1:n.*161G>C
ENST00000487525.5:c.*306G>C	ENSP00000431637.1:n.*306G>C
ENST00000578151.1:n.68G>C
ENST00000581221.5:n.248G>C
ENST00000583539.5:c.733G>C	ENSP00000463121.1:p.Ala245Pro
ENST00000584617.5:c.455G>C
ENST00000584804.1:c.28G>C	ENSP00000463658.1:p.Ala10Pro
NM_058216.2:c.733G>C	NP_478123.1:p.Ala245Pro
NR_103872.1:n.637G>C
XM_006722001.2:c.733G>C	XP_006722064.1:p.Ala245Pro
XM_006722002.2:c.733G>C	XP_006722065.1:p.Ala245Pro
XM_006722004.2:c.382G>C	XP_006722067.1:p.Ala128Pro
XM_006722005.2:c.382G>C	XP_006722068.1:p.Ala128Pro
XM_011525092.1:c.382G>C	XP_011523394.1:p.Ala128Pro
XM_011525093.1:c.382G>C	XP_011523395.1:p.Ala128Pro
XM_011525094.1:c.382G>C	XP_011523396.1:p.Ala128Pro
XR_934513.1:n.951G>C
XR_934514.1:n.951G>C
XM_006722001.4:c.733G>C	XP_006722064.1:p.Ala245Pro
XM_006722002.4:c.733G>C	XP_006722065.1:p.Ala245Pro
XM_006722004.3:c.382G>C	XP_006722067.1:p.Ala128Pro
XM_006722005.3:c.382G>C	XP_006722068.1:p.Ala128Pro
XM_011525092.2:c.382G>C	XP_011523394.1:p.Ala128Pro
XM_011525093.2:c.382G>C	XP_011523395.1:p.Ala128Pro
XM_011525094.2:c.382G>C	XP_011523396.1:p.Ala128Pro
XM_017024914.1:c.382G>C	XP_016880403.1:p.Ala128Pro
XM_017024915.1:c.382G>C	XP_016880404.1:p.Ala128Pro
XM_017024916.1:c.382G>C	XP_016880405.1:p.Ala128Pro
XM_017024917.1:c.382G>C	XP_016880406.1:p.Ala128Pro
XM_017024918.2:c.382G>C	XP_016880407.1:p.Ala128Pro
XM_017024919.1:c.382G>C	XP_016880408.1:p.Ala128Pro
XR_934513.3:n.1382G>C
XR_934514.3:n.1382G>C
NM_058216.3:c.733G>C MANE Select	NP_478123.1:p.Ala245Pro
NR_103872.2:n.608G>C