Canonical Allele Identifier: CA499730475

Gene: RAD51D

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35103298G>T , CM000679.2:g.35103298G>T	GRCh38
NC_000017.10:g.33430317G>T , CM000679.1:g.33430317G>T	GRCh37
NC_000017.9:g.30454430G>T	NCBI36
NG_031858.1:g.21572C>A , LRG_516:g.21572C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.559C>A	ENSP00000468273.3:p.Arg187=
ENST00000587405.6:c.337C>A	ENSP00000466478.2:p.Arg113=
ENST00000590016.6:c.754C>A	ENSP00000466399.1:p.Arg252=
ENST00000592577.6:c.337C>A	ENSP00000466839.2:p.Arg113=
ENST00000345365.11:c.694C>A MANE Select	ENSP00000338790.6:p.Arg232=
ENST00000335858.11:c.358C>A	ENSP00000338408.6:p.Arg120=
ENST00000345365.10:c.694C>A	ENSP00000338790.6:p.Arg232=
ENST00000394589.8:c.694C>A	ENSP00000378090.4:p.Arg232=
ENST00000460118.6:c.163C>A	ENSP00000464356.2:p.Arg55=
ENST00000586044.5:c.*425C>A	ENSP00000465584.1:n.*425C>A
ENST00000586210.5:c.*288C>A	ENSP00000465612.1:n.*288C>A
ENST00000587405.5:c.337C>A	ENSP00000466478.1:p.Arg113=
ENST00000587977.5:c.*434C>A	ENSP00000466587.1:n.*434C>A
ENST00000588372.5:c.*177C>A	ENSP00000468764.1:n.*177C>A
ENST00000588594.5:c.*290C>A	ENSP00000465366.1:n.*290C>A
ENST00000590016.5:c.754C>A	ENSP00000466399.1:p.Arg252=
ENST00000591723.5:c.163C>A	ENSP00000467986.1:p.Arg55=
ENST00000592181.1:c.337C>A	ENSP00000464799.1:p.Arg113=
ENST00000592577.5:c.700C>A	ENSP00000466839.1:p.Arg234=
ENST00000593039.5:c.217C>A	ENSP00000466834.1:p.Arg73=
NM_001142571.1:c.754C>A	NP_001136043.1:p.Arg252=
NM_002878.3:c.694C>A , LRG_516t1:c.694C>A	NP_002869.3:p.Arg232=
NM_133629.2:c.358C>A	NP_598332.1:p.Arg120=
NR_037711.1:n.831C>A
NR_037712.1:n.696C>A
NR_037714.1:n.446C>A
NM_001142571.2:c.754C>A	NP_001136043.1:p.Arg252=
NM_133629.3:c.358C>A	NP_598332.1:p.Arg120=
NR_037711.2:n.720C>A
NR_037712.2:n.585C>A
NM_002878.4:c.694C>A MANE Select	NP_002869.3:p.Arg232=