Canonical Allele Identifier: CA299916

Gene: RAD51D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35103455T>C , CM000679.2:g.35103455T>C	GRCh38
NC_000017.10:g.33430474T>C , CM000679.1:g.33430474T>C	GRCh37
NC_000017.9:g.30454587T>C	NCBI36
NG_031858.1:g.21415A>G , LRG_516:g.21415A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.531A>G	ENSP00000468273.3:p.Glu177=
ENST00000587405.6:c.309A>G	ENSP00000466478.2:p.Glu103=
ENST00000590016.6:c.726A>G	ENSP00000466399.1:p.Glu242=
ENST00000592577.6:c.309A>G	ENSP00000466839.2:p.Glu103=
ENST00000345365.11:c.666A>G MANE Select	ENSP00000338790.6:p.Glu222=
ENST00000335858.11:c.330A>G	ENSP00000338408.6:p.Glu110=
ENST00000345365.10:c.666A>G	ENSP00000338790.6:p.Glu222=
ENST00000394589.8:c.666A>G	ENSP00000378090.4:p.Glu222=
ENST00000460118.6:c.135A>G	ENSP00000464356.2:p.Glu45=
ENST00000586044.5:c.*397A>G	ENSP00000465584.1:n.*397A>G
ENST00000586210.5:c.*260A>G	ENSP00000465612.1:n.*260A>G
ENST00000587405.5:c.309A>G	ENSP00000466478.1:p.Glu103=
ENST00000587977.5:c.*406A>G	ENSP00000466587.1:n.*406A>G
ENST00000588372.5:c.*149A>G	ENSP00000468764.1:n.*149A>G
ENST00000588594.5:c.*262A>G	ENSP00000465366.1:n.*262A>G
ENST00000590016.5:c.726A>G	ENSP00000466399.1:p.Glu242=
ENST00000591723.5:c.135A>G	ENSP00000467986.1:p.Glu45=
ENST00000592181.1:c.309A>G	ENSP00000464799.1:p.Glu103=
ENST00000592577.5:c.672A>G	ENSP00000466839.1:p.Glu224=
ENST00000593039.5:c.189A>G	ENSP00000466834.1:p.Glu63=
NM_001142571.1:c.726A>G	NP_001136043.1:p.Glu242=
NM_002878.3:c.666A>G , LRG_516t1:c.666A>G	NP_002869.3:p.Glu222=
NM_133629.2:c.330A>G	NP_598332.1:p.Glu110=
NR_037711.1:n.803A>G
NR_037712.1:n.668A>G
NR_037714.1:n.418A>G
NM_001142571.2:c.726A>G	NP_001136043.1:p.Glu242=
NM_133629.3:c.330A>G	NP_598332.1:p.Glu110=
NR_037711.2:n.692A>G
NR_037712.2:n.557A>G
NM_002878.4:c.666A>G MANE Select	NP_002869.3:p.Glu222=