Canonical Allele Identifier: CA8677094

Gene: RAD51C

Linked Data

• dbSNP Id: rs768020569
• ExAC: 17:56769962 C / T
• gnomAD v2: 17-56769962-C-T
• gnomAD v4: 17-58692601-C-T
• MyVariant Identifiers: chr17:g.56769962C>T (hg19) ; chr17:g.58692601C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692601C>T , CM000679.2:g.58692601C>T	GRCh38
NC_000017.10:g.56769962C>T , CM000679.1:g.56769962C>T	GRCh37
NC_000017.9:g.54124961C>T	NCBI36
NG_023199.1:g.5000C>T , LRG_314:g.5000C>T
NG_047169.1:g.4479G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-291C>T	ENSP00000464056.2:n.-291C>T
ENST00000697675.1:n.29C>T
ENST00000697676.1:n.18C>T
ENST00000697677.1:n.16C>T
ENST00000697678.1:n.16C>T
ENST00000697679.1:n.9C>T
ENST00000697680.1:c.-43C>T	ENSP00000513392.1:n.-43C>T
ENST00000697681.1:c.-43C>T	ENSP00000513393.1:n.-43C>T
ENST00000697683.1:c.-43C>T	ENSP00000513395.1:n.-43C>T
ENST00000697684.1:n.18C>T
ENST00000697685.1:c.-43C>T	ENSP00000513396.1:n.-43C>T
ENST00000697686.1:c.-238C>T	ENSP00000513397.1:n.-238C>T
ENST00000697687.1:n.4C>T
ENST00000697688.1:n.4C>T
ENST00000337432.8:c.-43C>T	ENSP00000336701.4:n.-43C>T
ENST00000461271.5:c.-291C>T	ENSP00000464056.1:n.-291C>T
ENST00000487921.5:n.26C>T
ENST00000583539.5:c.-43C>T	ENSP00000463121.1:n.-43C>T
NM_002876.3:c.-43C>T	NP_002867.1:n.-43C>T
NM_058216.2:c.-43C>T	NP_478123.1:n.-43C>T
NR_103872.1:n.29C>T
NR_103873.1:n.29C>T
XM_006722001.2:c.-43C>T	XP_006722064.1:n.-43C>T
XM_006722002.2:c.-43C>T	XP_006722065.1:n.-43C>T
XM_006722004.2:c.-291C>T	XP_006722067.1:n.-291C>T
XM_006722005.2:c.-238C>T	XP_006722068.1:n.-238C>T
XM_011525092.1:c.-591C>T	XP_011523394.1:n.-591C>T
XM_011525093.1:c.-752C>T	XP_011523395.1:n.-752C>T
XR_934513.1:n.31C>T
XR_934514.1:n.31C>T
XM_006722001.4:c.-43C>T	XP_006722064.1:n.-43C>T
XM_006722002.4:c.-43C>T	XP_006722065.1:n.-43C>T
XM_006722004.3:c.-291C>T	XP_006722067.1:n.-291C>T
XM_006722005.3:c.-238C>T	XP_006722068.1:n.-238C>T
XM_017024914.1:c.-291C>T	XP_016880403.1:n.-291C>T
XM_017024917.1:c.-238C>T	XP_016880406.1:n.-238C>T
XR_934513.3:n.462C>T
XR_934514.3:n.462C>T