Canonical Allele Identifier: CA399086196

Gene: RAD51D

Linked Data

• ClinVar Variation Id: 472631
• ClinVar RCV Id: RCV000562807 ; RCV000540056 ; RCV001030588 ; RCV001171472 ; RCV003159903
• dbSNP Id: rs1403784434
• gnomAD v4: 17-35101038-T-A
• MyVariant Identifiers: chr17:g.33428057T>A (hg19) ; chr17:g.35101038T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35101038T>A , CM000679.2:g.35101038T>A	GRCh38
NC_000017.10:g.33428057T>A , CM000679.1:g.33428057T>A	GRCh37
NC_000017.9:g.30452170T>A	NCBI36
NG_031858.1:g.23832A>T , LRG_516:g.23832A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.769-2A>T	ENSP00000468273.3:n.769-2A>T
ENST00000587405.6:c.547-2A>T	ENSP00000466478.2:n.547-2A>T
ENST00000590016.6:c.964-2A>T	ENSP00000466399.1:n.964-2A>T
ENST00000592577.6:c.547-2A>T	ENSP00000466839.2:n.547-2A>T
ENST00000345365.11:c.904-2A>T MANE Select	ENSP00000338790.6:n.904-2A>T
ENST00000335858.11:c.568-2A>T	ENSP00000338408.6:n.568-2A>T
ENST00000345365.10:c.904-2A>T	ENSP00000338790.6:n.904-2A>T
ENST00000394589.8:c.904-2A>T	ENSP00000378090.4:n.904-2A>T
ENST00000460118.6:c.373-2A>T	ENSP00000464356.2:n.373-2A>T
ENST00000586044.5:c.*635-2A>T	ENSP00000465584.1:n.*635-2A>T
ENST00000586210.5:c.*498-2A>T	ENSP00000465612.1:n.*498-2A>T
ENST00000587977.5:c.*644-2A>T	ENSP00000466587.1:n.*644-2A>T
ENST00000588372.5:c.*387-2A>T	ENSP00000468764.1:n.*387-2A>T
ENST00000588594.5:c.*500-2A>T	ENSP00000465366.1:n.*500-2A>T
ENST00000590016.5:c.964-2A>T	ENSP00000466399.1:n.964-2A>T
ENST00000591723.5:c.372+163A>T	ENSP00000467986.1:n.372+163A>T
ENST00000592181.1:c.546+163A>T	ENSP00000464799.1:n.546+163A>T
ENST00000593039.5:c.426+163A>T	ENSP00000466834.1:n.426+163A>T
NM_001142571.1:c.964-2A>T	NP_001136043.1:n.964-2A>T
NM_002878.3:c.904-2A>T , LRG_516t1:c.904-2A>T	NP_002869.3:n.904-2A>T
NM_133629.2:c.568-2A>T	NP_598332.1:n.568-2A>T
NR_037711.1:n.1041-2A>T
NR_037712.1:n.906-2A>T
NR_037714.1:n.655+163A>T
NM_001142571.2:c.964-2A>T	NP_001136043.1:n.964-2A>T
NM_133629.3:c.568-2A>T	NP_598332.1:n.568-2A>T
NR_037711.2:n.930-2A>T
NR_037712.2:n.795-2A>T
NM_002878.4:c.904-2A>T MANE Select	NP_002869.3:n.904-2A>T