Canonical Allele Identifier: CA2267813908

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692587C= , CM000679.2:g.58692587C=	GRCh38
NC_000017.10:g.56769948C= , CM000679.1:g.56769948C=	GRCh37
NC_000017.9:g.54124947C=	NCBI36
NG_023199.1:g.4986C= , LRG_314:g.4986C=
NG_047169.1:g.4493G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-305C=	ENSP00000464056.2:n.-305C=
ENST00000697675.1:n.15C=
ENST00000697676.1:n.4C=
ENST00000697677.1:n.2C=
ENST00000697678.1:n.2C=
ENST00000697683.1:c.-57C=	ENSP00000513395.1:n.-57C=
ENST00000697684.1:n.4C=
ENST00000337432.8:c.-57C=	ENSP00000336701.4:n.-57C=
ENST00000461271.5:c.-305C=	ENSP00000464056.1:n.-305C=
ENST00000487921.5:n.12C=
ENST00000583539.5:c.-57C=	ENSP00000463121.1:n.-57C=
NM_002876.3:c.-57C=	NP_002867.1:n.-57C=
NM_058216.2:c.-57C=	NP_478123.1:n.-57C=
NR_103872.1:n.15C=
NR_103873.1:n.15C=
XM_006722001.2:c.-57C=	XP_006722064.1:n.-57C=
XM_006722002.2:c.-57C=	XP_006722065.1:n.-57C=
XM_006722004.2:c.-305C=	XP_006722067.1:n.-305C=
XM_006722005.2:c.-252C=	XP_006722068.1:n.-252C=
XR_934513.1:n.17C=
XR_934514.1:n.17C=
XM_006722001.4:c.-57C=	XP_006722064.1:n.-57C=
XM_006722002.4:c.-57C=	XP_006722065.1:n.-57C=
XM_006722004.3:c.-305C=	XP_006722067.1:n.-305C=
XM_006722005.3:c.-252C=	XP_006722068.1:n.-252C=
XM_017024914.1:c.-305C=	XP_016880403.1:n.-305C=
XM_017024917.1:c.-252C=	XP_016880406.1:n.-252C=
XR_934513.3:n.448C=
XR_934514.3:n.448C=