Canonical Allele Identifier: CA2638988635

Gene: RAD51C

Linked Data

• gnomAD v4: 17-58692580-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692580C>A , CM000679.2:g.58692580C>A	GRCh38
NC_000017.10:g.56769941C>A , CM000679.1:g.56769941C>A	GRCh37
NC_000017.9:g.54124940C>A	NCBI36
NG_023199.1:g.4979C>A , LRG_314:g.4979C>A
NG_047169.1:g.4500G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.-312C>A	ENSP00000464056.2:n.-312C>A
ENST00000697675.1:n.8C>A
ENST00000697683.1:c.-64C>A	ENSP00000513395.1:n.-64C>A
ENST00000337432.8:c.-64C>A	ENSP00000336701.4:n.-64C>A
ENST00000461271.5:c.-312C>A	ENSP00000464056.1:n.-312C>A
ENST00000487921.5:n.5C>A
ENST00000583539.5:c.-64C>A	ENSP00000463121.1:n.-64C>A
NM_002876.3:c.-64C>A	NP_002867.1:n.-64C>A
NM_058216.2:c.-64C>A	NP_478123.1:n.-64C>A
NR_103872.1:n.8C>A
NR_103873.1:n.8C>A
XM_006722001.2:c.-64C>A	XP_006722064.1:n.-64C>A
XM_006722002.2:c.-64C>A	XP_006722065.1:n.-64C>A
XM_006722004.2:c.-312C>A	XP_006722067.1:n.-312C>A
XM_006722005.2:c.-259C>A	XP_006722068.1:n.-259C>A
XR_934513.1:n.10C>A
XR_934514.1:n.10C>A
XM_006722001.4:c.-64C>A	XP_006722064.1:n.-64C>A
XM_006722002.4:c.-64C>A	XP_006722065.1:n.-64C>A
XM_006722004.3:c.-312C>A	XP_006722067.1:n.-312C>A
XM_006722005.3:c.-259C>A	XP_006722068.1:n.-259C>A
XM_017024914.1:c.-312C>A	XP_016880403.1:n.-312C>A
XM_017024917.1:c.-259C>A	XP_016880406.1:n.-259C>A
XR_934513.3:n.441C>A
XR_934514.3:n.441C>A