Canonical Allele Identifier: CA2011734945

Gene: RAD52

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.913286C= , CM000674.2:g.913286C=	GRCh38
NC_000012.11:g.1022452C= , CM000674.1:g.1022452C=	GRCh37
NC_000012.10:g.892713C=	NCBI36
NG_007984.2:g.165228C=
NG_017078.1:g.41412G=
NG_007984.3:g.165228C=
NG_017078.2:g.81756G=

Transcript Alleles

HGVS	Amino-acid Change
NM_134424.4:c.*105G= MANE Select	NP_602296.2:n.*105G=
ENST00000358495.8:c.*105G= MANE Select	ENSP00000351284.3:n.*105G=
NM_001297419.1:c.*105G=	NP_001284348.1:n.*105G=
NM_001297421.1:c.*105G=	NP_001284350.1:n.*105G=
NM_001297421.2:c.*105G=	NP_001284350.1:n.*105G=
NM_134424.3:c.*105G=	NP_602296.2:n.*105G=
NR_123713.1:n.1783G=
NR_123713.2:n.1755G=
ENST00000228345.9:n.1695G=
ENST00000358495.7:c.*105G=	ENSP00000351284.3:n.*105G=
ENST00000430095.6:c.*105G=	ENSP00000387901.2:n.*105G=
ENST00000468231.5:c.*1148G=	ENSP00000434703.1:n.*1148G=
ENST00000481052.5:n.1673G=
ENST00000488642.6:n.1885G=
ENST00000535376.5:n.756G=
XM_005253720.3:c.*105G=	XP_005253777.1:n.*105G=
XM_005253720.5:c.*105G=	XP_005253777.1:n.*105G=
XM_005253721.2:c.*105G=	XP_005253778.1:n.*105G=
XM_011520990.1:c.*105G=	XP_011519292.1:n.*105G=
XM_011520990.2:c.*105G=	XP_011519292.1:n.*105G=
XM_011520991.1:c.*105G=	XP_011519293.1:n.*105G=
XM_011520991.2:c.*105G=	XP_011519293.1:n.*105G=
XM_011520992.1:c.*105G=	XP_011519294.1:n.*105G=
XM_011520995.1:c.*105G=	XP_011519297.1:n.*105G=
XM_011520995.3:c.*105G=	XP_011519297.1:n.*105G=
XM_017019769.1:c.*105G=	XP_016875258.1:n.*105G=
XM_017019770.1:c.*105G=	XP_016875259.1:n.*105G=
XR_001748836.1:n.1504G=
XR_001748837.1:n.1501G=
XR_001748838.2:n.1603G=
XR_001748839.1:n.1501G=
XR_931521.1:n.1449G=
XR_931522.1:n.1524G=
XR_931522.2:n.1524G=