Canonical Allele Identifier: CA2638988600

Gene: RAD51C

Linked Data

• gnomAD v4: 17-58692573-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692573G>A , CM000679.2:g.58692573G>A	GRCh38
NC_000017.10:g.56769934G>A , CM000679.1:g.56769934G>A	GRCh37
NC_000017.9:g.54124933G>A	NCBI36
NG_023199.1:g.4972G>A , LRG_314:g.4972G>A
NG_047169.1:g.4507C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-319G>A	ENSP00000464056.2:n.-319G>A
ENST00000697675.1:n.1G>A
ENST00000337432.8:c.-71G>A	ENSP00000336701.4:n.-71G>A
ENST00000461271.5:c.-319G>A	ENSP00000464056.1:n.-319G>A
ENST00000583539.5:c.-71G>A	ENSP00000463121.1:n.-71G>A
NM_002876.3:c.-71G>A	NP_002867.1:n.-71G>A
NM_058216.2:c.-71G>A	NP_478123.1:n.-71G>A
NR_103872.1:n.1G>A
NR_103873.1:n.1G>A
XM_006722001.2:c.-71G>A	XP_006722064.1:n.-71G>A
XM_006722002.2:c.-71G>A	XP_006722065.1:n.-71G>A
XM_006722005.2:c.-266G>A	XP_006722068.1:n.-266G>A
XR_934513.1:n.3G>A
XR_934514.1:n.3G>A
XM_006722001.4:c.-71G>A	XP_006722064.1:n.-71G>A
XM_006722002.4:c.-71G>A	XP_006722065.1:n.-71G>A
XM_006722005.3:c.-266G>A	XP_006722068.1:n.-266G>A
XM_017024917.1:c.-266G>A	XP_016880406.1:n.-266G>A
XR_934513.3:n.434G>A
XR_934514.3:n.434G>A