Canonical Allele Identifier: CA399086041

Gene: RAD51D

Linked Data

• ClinVar Variation Id: 472633
• ClinVar RCV Id: RCV000532608 ; RCV001185232
• dbSNP Id: rs1555566935
• MyVariant Identifiers: chr17:g.33427982T>G (hg19) ; chr17:g.35100963T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35100963T>G , CM000679.2:g.35100963T>G	GRCh38
NC_000017.10:g.33427982T>G , CM000679.1:g.33427982T>G	GRCh37
NC_000017.9:g.30452095T>G	NCBI36
NG_031858.1:g.23907A>C , LRG_516:g.23907A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.842A>C	ENSP00000468273.3:p.Asp281Ala
ENST00000587405.6:c.620A>C	ENSP00000466478.2:p.Asp207Ala
ENST00000590016.6:c.1037A>C	ENSP00000466399.1:p.Asp346Ala
ENST00000592577.6:c.620A>C	ENSP00000466839.2:p.Asp207Ala
ENST00000345365.11:c.977A>C MANE Select	ENSP00000338790.6:p.Asp326Ala
ENST00000335858.11:c.641A>C	ENSP00000338408.6:p.Asp214Ala
ENST00000345365.10:c.977A>C	ENSP00000338790.6:p.Asp326Ala
ENST00000394589.8:c.977A>C	ENSP00000378090.4:p.Asp326Ala
ENST00000460118.6:c.446A>C	ENSP00000464356.2:p.Asp149Ala
ENST00000586044.5:c.*708A>C	ENSP00000465584.1:n.*708A>C
ENST00000586210.5:c.*571A>C	ENSP00000465612.1:n.*571A>C
ENST00000587977.5:c.*717A>C	ENSP00000466587.1:n.*717A>C
ENST00000588372.5:c.*460A>C	ENSP00000468764.1:n.*460A>C
ENST00000588594.5:c.*573A>C	ENSP00000465366.1:n.*573A>C
ENST00000590016.5:c.1037A>C	ENSP00000466399.1:p.Asp346Ala
ENST00000591723.5:c.372+238A>C	ENSP00000467986.1:n.372+238A>C
ENST00000592181.1:c.546+238A>C	ENSP00000464799.1:n.546+238A>C
ENST00000593039.5:c.426+238A>C	ENSP00000466834.1:n.426+238A>C
NM_001142571.1:c.1037A>C	NP_001136043.1:p.Asp346Ala
NM_002878.3:c.977A>C , LRG_516t1:c.977A>C	NP_002869.3:p.Asp326Ala
NM_133629.2:c.641A>C	NP_598332.1:p.Asp214Ala
NR_037711.1:n.1114A>C
NR_037712.1:n.979A>C
NR_037714.1:n.655+238A>C
NM_001142571.2:c.1037A>C	NP_001136043.1:p.Asp346Ala
NM_133629.3:c.641A>C	NP_598332.1:p.Asp214Ala
NR_037711.2:n.1003A>C
NR_037712.2:n.868A>C
NM_002878.4:c.977A>C MANE Select	NP_002869.3:p.Asp326Ala