Canonical Allele Identifier: CA399087669

Gene: RAD51D

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.559C>G	ENSP00000468273.3:p.Arg187Gly
ENST00000587405.6:c.337C>G	ENSP00000466478.2:p.Arg113Gly
ENST00000590016.6:c.754C>G	ENSP00000466399.1:p.Arg252Gly
ENST00000592577.6:c.337C>G	ENSP00000466839.2:p.Arg113Gly
ENST00000345365.11:c.694C>G MANE Select	ENSP00000338790.6:p.Arg232Gly
ENST00000335858.11:c.358C>G	ENSP00000338408.6:p.Arg120Gly
ENST00000345365.10:c.694C>G	ENSP00000338790.6:p.Arg232Gly
ENST00000394589.8:c.694C>G	ENSP00000378090.4:p.Arg232Gly
ENST00000460118.6:c.163C>G	ENSP00000464356.2:p.Arg55Gly
ENST00000586044.5:c.*425C>G	ENSP00000465584.1:n.*425C>G
ENST00000586210.5:c.*288C>G	ENSP00000465612.1:n.*288C>G
ENST00000587405.5:c.337C>G	ENSP00000466478.1:p.Arg113Gly
ENST00000587977.5:c.*434C>G	ENSP00000466587.1:n.*434C>G
ENST00000588372.5:c.*177C>G	ENSP00000468764.1:n.*177C>G
ENST00000588594.5:c.*290C>G	ENSP00000465366.1:n.*290C>G
ENST00000590016.5:c.754C>G	ENSP00000466399.1:p.Arg252Gly
ENST00000591723.5:c.163C>G	ENSP00000467986.1:p.Arg55Gly
ENST00000592181.1:c.337C>G	ENSP00000464799.1:p.Arg113Gly
ENST00000592577.5:c.700C>G	ENSP00000466839.1:p.Arg234Gly
ENST00000593039.5:c.217C>G	ENSP00000466834.1:p.Arg73Gly
NM_001142571.1:c.754C>G	NP_001136043.1:p.Arg252Gly
NM_002878.3:c.694C>G , LRG_516t1:c.694C>G	NP_002869.3:p.Arg232Gly
NM_133629.2:c.358C>G	NP_598332.1:p.Arg120Gly
NR_037711.1:n.831C>G
NR_037712.1:n.696C>G
NR_037714.1:n.446C>G
NM_001142571.2:c.754C>G	NP_001136043.1:p.Arg252Gly
NM_133629.3:c.358C>G	NP_598332.1:p.Arg120Gly
NR_037711.2:n.720C>G
NR_037712.2:n.585C>G
NM_002878.4:c.694C>G MANE Select	NP_002869.3:p.Arg232Gly