Canonical Allele Identifier: CA8499336

Gene: RAD51D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35101269C>T , CM000679.2:g.35101269C>T	GRCh38
NC_000017.10:g.33428288C>T , CM000679.1:g.33428288C>T	GRCh37
NC_000017.9:g.30452401C>T	NCBI36
NG_031858.1:g.23601G>A , LRG_516:g.23601G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002878.4:c.835G>A MANE Select	NP_002869.3:p.Asp279Asn
ENST00000345365.11:c.835G>A MANE Select	ENSP00000338790.6:p.Asp279Asn
NM_001142571.1:c.895G>A	NP_001136043.1:p.Asp299Asn
NM_001142571.2:c.895G>A	NP_001136043.1:p.Asp299Asn
NM_002878.3:c.835G>A , LRG_516t1:c.835G>A	NP_002869.3:p.Asp279Asn
NM_133629.2:c.499G>A	NP_598332.1:p.Asp167Asn
NM_133629.3:c.499G>A	NP_598332.1:p.Asp167Asn
NR_037711.1:n.972G>A
NR_037711.2:n.861G>A
NR_037712.1:n.837G>A
NR_037712.2:n.726G>A
NR_037714.1:n.587G>A
ENST00000335858.11:c.499G>A	ENSP00000338408.6:p.Asp167Asn
ENST00000345365.10:c.835G>A	ENSP00000338790.6:p.Asp279Asn
ENST00000394589.8:c.835G>A	ENSP00000378090.4:p.Asp279Asn
ENST00000460118.6:c.304G>A	ENSP00000464356.2:p.Asp102Asn
ENST00000586044.5:c.*566G>A	ENSP00000465584.1:n.*566G>A
ENST00000586186.3:c.700G>A	ENSP00000468273.3:p.Asp234Asn
ENST00000586210.5:c.*429G>A	ENSP00000465612.1:n.*429G>A
ENST00000587405.6:c.478G>A	ENSP00000466478.2:p.Asp160Asn
ENST00000587977.5:c.*575G>A	ENSP00000466587.1:n.*575G>A
ENST00000588372.5:c.*318G>A	ENSP00000468764.1:n.*318G>A
ENST00000588594.5:c.*431G>A	ENSP00000465366.1:n.*431G>A
ENST00000590016.5:c.895G>A	ENSP00000466399.1:p.Asp299Asn
ENST00000590016.6:c.895G>A	ENSP00000466399.1:p.Asp299Asn
ENST00000591723.5:c.304G>A	ENSP00000467986.1:p.Asp102Asn
ENST00000592181.1:c.478G>A	ENSP00000464799.1:p.Asp160Asn
ENST00000592577.6:c.478G>A	ENSP00000466839.2:p.Asp160Asn
ENST00000593039.5:c.358G>A	ENSP00000466834.1:p.Asp120Asn