Canonical Allele Identifier: CA16615706

Gene: RAD51D

Linked Data

• ClinVar Variation Id: 410561
• ClinVar RCV Id: RCV000476191 ; RCV000580855 ; RCV001797727 ; RCV002279232
• dbSNP Id: rs1060502959
• gnomAD v4: 17-35101203-G-A
• MyVariant Identifiers: chr17:g.33428222G>A (hg19) ; chr17:g.35101203G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35101203G>A , CM000679.2:g.35101203G>A	GRCh38
NC_000017.10:g.33428222G>A , CM000679.1:g.33428222G>A	GRCh37
NC_000017.9:g.30452335G>A	NCBI36
NG_031858.1:g.23667C>T , LRG_516:g.23667C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.766C>T	ENSP00000468273.3:p.Gln256Ter
ENST00000587405.6:c.544C>T	ENSP00000466478.2:p.Gln182Ter
ENST00000590016.6:c.961C>T	ENSP00000466399.1:p.Gln321Ter
ENST00000592577.6:c.544C>T	ENSP00000466839.2:p.Gln182Ter
ENST00000345365.11:c.901C>T MANE Select	ENSP00000338790.6:p.Gln301Ter
ENST00000335858.11:c.565C>T	ENSP00000338408.6:p.Gln189Ter
ENST00000345365.10:c.901C>T	ENSP00000338790.6:p.Gln301Ter
ENST00000394589.8:c.901C>T	ENSP00000378090.4:p.Gln301Ter
ENST00000460118.6:c.370C>T	ENSP00000464356.2:p.Gln124Ter
ENST00000586044.5:c.*632C>T	ENSP00000465584.1:n.*632C>T
ENST00000586210.5:c.*495C>T	ENSP00000465612.1:n.*495C>T
ENST00000587977.5:c.*641C>T	ENSP00000466587.1:n.*641C>T
ENST00000588372.5:c.*384C>T	ENSP00000468764.1:n.*384C>T
ENST00000588594.5:c.*497C>T	ENSP00000465366.1:n.*497C>T
ENST00000590016.5:c.961C>T	ENSP00000466399.1:p.Gln321Ter
ENST00000591723.5:c.370C>T	ENSP00000467986.1:p.Gln124Ter
ENST00000592181.1:c.544C>T	ENSP00000464799.1:p.Gln182Ter
ENST00000593039.5:c.424C>T	ENSP00000466834.1:p.Gln142Ter
NM_001142571.1:c.961C>T	NP_001136043.1:p.Gln321Ter
NM_002878.3:c.901C>T , LRG_516t1:c.901C>T	NP_002869.3:p.Gln301Ter
NM_133629.2:c.565C>T	NP_598332.1:p.Gln189Ter
NR_037711.1:n.1038C>T
NR_037712.1:n.903C>T
NR_037714.1:n.653C>T
NM_001142571.2:c.961C>T	NP_001136043.1:p.Gln321Ter
NM_133629.3:c.565C>T	NP_598332.1:p.Gln189Ter
NR_037711.2:n.927C>T
NR_037712.2:n.792C>T
NM_002878.4:c.901C>T MANE Select	NP_002869.3:p.Gln301Ter