Canonical Allele Identifier: CA2267813919

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692597A= , CM000679.2:g.58692597A=	GRCh38
NC_000017.10:g.56769958A= , CM000679.1:g.56769958A=	GRCh37
NC_000017.9:g.54124957A=	NCBI36
NG_023199.1:g.4996A= , LRG_314:g.4996A=
NG_047169.1:g.4483T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-295A=	ENSP00000464056.2:n.-295A=
ENST00000697675.1:n.25A=
ENST00000697676.1:n.14A=
ENST00000697677.1:n.12A=
ENST00000697678.1:n.12A=
ENST00000697679.1:n.5A=
ENST00000697680.1:c.-47A=	ENSP00000513392.1:n.-47A=
ENST00000697681.1:c.-47A=	ENSP00000513393.1:n.-47A=
ENST00000697683.1:c.-47A=	ENSP00000513395.1:n.-47A=
ENST00000697684.1:n.14A=
ENST00000697685.1:c.-47A=	ENSP00000513396.1:n.-47A=
ENST00000697686.1:c.-242A=	ENSP00000513397.1:n.-242A=
ENST00000337432.8:c.-47A=	ENSP00000336701.4:n.-47A=
ENST00000461271.5:c.-295A=	ENSP00000464056.1:n.-295A=
ENST00000487921.5:n.22A=
ENST00000583539.5:c.-47A=	ENSP00000463121.1:n.-47A=
NM_002876.3:c.-47A=	NP_002867.1:n.-47A=
NM_058216.2:c.-47A=	NP_478123.1:n.-47A=
NR_103872.1:n.25A=
NR_103873.1:n.25A=
XM_006722001.2:c.-47A=	XP_006722064.1:n.-47A=
XM_006722002.2:c.-47A=	XP_006722065.1:n.-47A=
XM_006722004.2:c.-295A=	XP_006722067.1:n.-295A=
XM_006722005.2:c.-242A=	XP_006722068.1:n.-242A=
XM_011525092.1:c.-595A=	XP_011523394.1:n.-595A=
XM_011525093.1:c.-756A=	XP_011523395.1:n.-756A=
XR_934513.1:n.27A=
XR_934514.1:n.27A=
XM_006722001.4:c.-47A=	XP_006722064.1:n.-47A=
XM_006722002.4:c.-47A=	XP_006722065.1:n.-47A=
XM_006722004.3:c.-295A=	XP_006722067.1:n.-295A=
XM_006722005.3:c.-242A=	XP_006722068.1:n.-242A=
XM_017024914.1:c.-295A=	XP_016880403.1:n.-295A=
XM_017024917.1:c.-242A=	XP_016880406.1:n.-242A=
XR_934513.3:n.458A=
XR_934514.3:n.458A=