Canonical Allele Identifier: CA230772

Gene: RAD52

Linked Data

• ClinVar Variation Id: 127042
• ClinVar RCV Id: RCV000114908
• dbSNP Id: rs104895055
• MyVariant Identifiers: chr12:g.1021565A>C (hg19) ; chr12:g.912399A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.912399A>C , CM000674.2:g.912399A>C	GRCh38
NC_000012.11:g.1021565A>C , CM000674.1:g.1021565A>C	GRCh37
NC_000012.10:g.891826A>C	NCBI36
NG_007984.2:g.164341A>C
NG_017078.1:g.42299T>G
NG_007984.3:g.164341A>C
NG_017078.2:g.82643T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358495.8:c.*992T>G MANE Select	ENSP00000351284.3:n.*992T>G
ENST00000228345.9:n.2582T>G
ENST00000358495.7:c.*992T>G	ENSP00000351284.3:n.*992T>G
NM_001297419.1:c.*992T>G	NP_001284348.1:n.*992T>G
NM_001297421.1:c.*992T>G	NP_001284350.1:n.*992T>G
NM_134424.3:c.*992T>G	NP_602296.2:n.*992T>G
NR_123713.1:n.2670T>G
XM_005253720.3:c.*992T>G	XP_005253777.1:n.*992T>G
XM_005253721.2:c.*992T>G	XP_005253778.1:n.*992T>G
XM_011520990.1:c.*992T>G	XP_011519292.1:n.*992T>G
XM_011520991.1:c.*992T>G	XP_011519293.1:n.*992T>G
XM_011520992.1:c.*992T>G	XP_011519294.1:n.*992T>G
XM_011520995.1:c.*992T>G	XP_011519297.1:n.*992T>G
XR_931521.1:n.2336T>G
XR_931522.1:n.2411T>G
XM_005253720.5:c.*992T>G	XP_005253777.1:n.*992T>G
XM_011520990.2:c.*992T>G	XP_011519292.1:n.*992T>G
XM_011520991.2:c.*992T>G	XP_011519293.1:n.*992T>G
XM_011520995.3:c.*992T>G	XP_011519297.1:n.*992T>G
XM_017019769.1:c.*992T>G	XP_016875258.1:n.*992T>G
XM_017019770.1:c.*992T>G	XP_016875259.1:n.*992T>G
XR_001748836.1:n.2391T>G
XR_001748837.1:n.2388T>G
XR_001748838.2:n.2490T>G
XR_001748839.1:n.2388T>G
XR_931522.2:n.2411T>G
NM_134424.4:c.*992T>G MANE Select	NP_602296.2:n.*992T>G
NM_001297421.2:c.*992T>G	NP_001284350.1:n.*992T>G
NR_123713.2:n.2642T>G