Canonical Allele Identifier: CA2011733364

Gene: RAD52

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.912349T= , CM000674.2:g.912349T=	GRCh38
NC_000012.11:g.1021515T= , CM000674.1:g.1021515T=	GRCh37
NC_000012.10:g.891776T=	NCBI36
NG_007984.2:g.164291T=
NG_017078.1:g.42349A=
NG_007984.3:g.164291T=
NG_017078.2:g.82693A=

Transcript Alleles

HGVS	Amino-acid Change
NM_134424.4:c.*1042A= MANE Select	NP_602296.2:n.*1042A=
ENST00000358495.8:c.*1042A= MANE Select	ENSP00000351284.3:n.*1042A=
NM_001297419.1:c.*1042A=	NP_001284348.1:n.*1042A=
NM_001297421.1:c.*1042A=	NP_001284350.1:n.*1042A=
NM_001297421.2:c.*1042A=	NP_001284350.1:n.*1042A=
NM_134424.3:c.*1042A=	NP_602296.2:n.*1042A=
NR_123713.1:n.2720A=
NR_123713.2:n.2692A=
ENST00000228345.9:n.2632A=
ENST00000358495.7:c.*1042A=	ENSP00000351284.3:n.*1042A=
XM_005253720.3:c.*1042A=	XP_005253777.1:n.*1042A=
XM_005253720.5:c.*1042A=	XP_005253777.1:n.*1042A=
XM_005253721.2:c.*1042A=	XP_005253778.1:n.*1042A=
XM_011520990.1:c.*1042A=	XP_011519292.1:n.*1042A=
XM_011520990.2:c.*1042A=	XP_011519292.1:n.*1042A=
XM_011520991.1:c.*1042A=	XP_011519293.1:n.*1042A=
XM_011520991.2:c.*1042A=	XP_011519293.1:n.*1042A=
XM_011520992.1:c.*1042A=	XP_011519294.1:n.*1042A=
XM_011520995.1:c.*1042A=	XP_011519297.1:n.*1042A=
XM_011520995.3:c.*1042A=	XP_011519297.1:n.*1042A=
XM_017019769.1:c.*1042A=	XP_016875258.1:n.*1042A=
XM_017019770.1:c.*1042A=	XP_016875259.1:n.*1042A=
XR_001748836.1:n.2441A=
XR_001748837.1:n.2438A=
XR_001748838.2:n.2540A=
XR_001748839.1:n.2438A=
XR_931521.1:n.2386A=
XR_931522.1:n.2461A=
XR_931522.2:n.2461A=