Canonical Allele Identifier: CA399086803

Gene: RAD51D

Linked Data

• dbSNP Id: rs1597856016
• MyVariant Identifiers: chr17:g.33428319C>T (hg19) ; chr17:g.35101300C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35101300C>T , CM000679.2:g.35101300C>T	GRCh38
NC_000017.10:g.33428319C>T , CM000679.1:g.33428319C>T	GRCh37
NC_000017.9:g.30452432C>T	NCBI36
NG_031858.1:g.23570G>A , LRG_516:g.23570G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.669G>A	ENSP00000468273.3:p.Trp223Ter
ENST00000587405.6:c.447G>A	ENSP00000466478.2:p.Trp149Ter
ENST00000590016.6:c.864G>A	ENSP00000466399.1:p.Trp288Ter
ENST00000592577.6:c.447G>A	ENSP00000466839.2:p.Trp149Ter
ENST00000345365.11:c.804G>A MANE Select	ENSP00000338790.6:p.Trp268Ter
ENST00000335858.11:c.468G>A	ENSP00000338408.6:p.Trp156Ter
ENST00000345365.10:c.804G>A	ENSP00000338790.6:p.Trp268Ter
ENST00000394589.8:c.804G>A	ENSP00000378090.4:p.Trp268Ter
ENST00000460118.6:c.273G>A	ENSP00000464356.2:p.Trp91Ter
ENST00000586044.5:c.*535G>A	ENSP00000465584.1:n.*535G>A
ENST00000586210.5:c.*398G>A	ENSP00000465612.1:n.*398G>A
ENST00000587977.5:c.*544G>A	ENSP00000466587.1:n.*544G>A
ENST00000588372.5:c.*287G>A	ENSP00000468764.1:n.*287G>A
ENST00000588594.5:c.*400G>A	ENSP00000465366.1:n.*400G>A
ENST00000590016.5:c.864G>A	ENSP00000466399.1:p.Trp288Ter
ENST00000591723.5:c.273G>A	ENSP00000467986.1:p.Trp91Ter
ENST00000592181.1:c.447G>A	ENSP00000464799.1:p.Trp149Ter
ENST00000593039.5:c.327G>A	ENSP00000466834.1:p.Trp109Ter
NM_001142571.1:c.864G>A	NP_001136043.1:p.Trp288Ter
NM_002878.3:c.804G>A , LRG_516t1:c.804G>A	NP_002869.3:p.Trp268Ter
NM_133629.2:c.468G>A	NP_598332.1:p.Trp156Ter
NR_037711.1:n.941G>A
NR_037712.1:n.806G>A
NR_037714.1:n.556G>A
NM_001142571.2:c.864G>A	NP_001136043.1:p.Trp288Ter
NM_133629.3:c.468G>A	NP_598332.1:p.Trp156Ter
NR_037711.2:n.830G>A
NR_037712.2:n.695G>A
NM_002878.4:c.804G>A MANE Select	NP_002869.3:p.Trp268Ter