Canonical Allele Identifier: CA399091369

Gene: RAD51D

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35118562C>G , CM000679.2:g.35118562C>G	GRCh38
NC_000017.10:g.33445581C>G , CM000679.1:g.33445581C>G	GRCh37
NC_000017.9:g.30469694C>G	NCBI36
NG_031858.1:g.6308G>C , LRG_516:g.6308G>C
NG_054719.1:g.1984C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.202G>C	ENSP00000468273.3:p.Gly68Arg
ENST00000587405.6:c.-95+2729G>C	ENSP00000466478.2:n.-95+2729G>C
ENST00000590016.6:c.144+549G>C	ENSP00000466399.1:n.144+549G>C
ENST00000590631.2:n.436+549G>C
ENST00000592577.6:c.-156G>C	ENSP00000466839.2:n.-156G>C
ENST00000345365.11:c.202G>C MANE Select	ENSP00000338790.6:p.Gly68Arg
ENST00000335858.11:c.144+549G>C	ENSP00000338408.6:n.144+549G>C
ENST00000345365.10:c.202G>C	ENSP00000338790.6:p.Gly68Arg
ENST00000394589.8:c.202G>C	ENSP00000378090.4:p.Gly68Arg
ENST00000415064.6:n.352G>C
ENST00000460118.6:c.-208+549G>C	ENSP00000464356.2:n.-208+549G>C
ENST00000585343.5:c.105G>C
ENST00000585947.5:n.159+2729G>C
ENST00000585982.5:n.239+549G>C
ENST00000586044.5:c.144+549G>C	ENSP00000465584.1:n.144+549G>C
ENST00000586186.2:c.105G>C
ENST00000586210.5:c.202G>C	ENSP00000465612.1:p.Gly68Arg
ENST00000587405.5:c.-95+2729G>C	ENSP00000466478.1:n.-95+2729G>C
ENST00000587977.5:c.202G>C	ENSP00000466587.1:p.Gly68Arg
ENST00000587982.5:n.191+2729G>C
ENST00000588372.5:c.-95+2729G>C	ENSP00000468764.1:n.-95+2729G>C
ENST00000588594.5:c.144+549G>C	ENSP00000465366.1:n.144+549G>C
ENST00000589506.1:n.355+549G>C
ENST00000590016.5:c.144+549G>C	ENSP00000466399.1:n.144+549G>C
ENST00000590631.1:c.-52+549G>C	ENSP00000465033.1:n.-52+549G>C
ENST00000591723.5:c.-134+2729G>C	ENSP00000467986.1:n.-134+2729G>C
ENST00000592181.1:c.-95+549G>C	ENSP00000464799.1:n.-95+549G>C
ENST00000592430.5:n.232+2729G>C
ENST00000592577.5:c.208G>C	ENSP00000466839.1:p.Gly70Arg
ENST00000592850.5:c.105G>C
ENST00000592928.2:n.105G>C
ENST00000593039.5:c.3+2729G>C	ENSP00000466834.1:n.3+2729G>C
NM_001142571.1:c.144+549G>C	NP_001136043.1:n.144+549G>C
NM_002878.3:c.202G>C , LRG_516t1:c.202G>C	NP_002869.3:p.Gly68Arg
NM_133629.2:c.144+549G>C	NP_598332.1:n.144+549G>C
NR_037711.1:n.400+549G>C
NR_037712.1:n.400+549G>C
NR_037714.1:n.232+2729G>C
NM_001142571.2:c.144+549G>C	NP_001136043.1:n.144+549G>C
NM_133629.3:c.144+549G>C	NP_598332.1:n.144+549G>C
NR_037711.2:n.289+549G>C
NR_037712.2:n.289+549G>C
NM_002878.4:c.202G>C MANE Select	NP_002869.3:p.Gly68Arg