Canonical Allele Identifier: CA16042160
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 371921
ClinVar RCV Id: RCV000410439 RCV001018078
dbSNP Id: rs1057517586
gnomAD v4: 17-35119169-AC-A
MyVariant Identifiers: chr17:g.33446189del (hg19) chr17:g.35119170del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35119171del , CM000679.2:g.35119171del GRCh38
NC_000017.10:g.33446190del , CM000679.1:g.33446190del GRCh37
NC_000017.9:g.30470303del NCBI36
NG_031858.1:g.5700del , LRG_516:g.5700del
NG_054719.1:g.2593del

Transcript Alleles

HGVS Amino-acid change
ENST00000586186.3:c.85del ENSP00000468273.3:p.Val29TrpfsTer11
ENST00000587405.6:c.-95+2121del ENSP00000466478.2:n.-95+2121del
ENST00000590016.6:c.85del ENSP00000466399.1:p.Val29TrpfsTer11
ENST00000590631.2:n.377del
ENST00000592577.6:c.-273del ENSP00000466839.2:n.-273del
ENST00000345365.11:c.85del MANE Select ENSP00000338790.6:p.Val29TrpfsTer11
ENST00000335858.11:c.85del ENSP00000338408.6:p.Val29TrpfsTer11
ENST00000345365.10:c.85del ENSP00000338790.6:p.Val29TrpfsTer11
ENST00000394589.8:c.85del ENSP00000378090.4:p.Val29TrpfsTer11
ENST00000415064.6:n.235del
ENST00000460118.6:c.-267del ENSP00000464356.2:n.-267del
ENST00000585947.5:n.159+2121del
ENST00000585982.5:n.180del
ENST00000586044.5:c.85del ENSP00000465584.1:p.Val29TrpfsTer11
ENST00000586210.5:c.85del ENSP00000465612.1:p.Val29TrpfsTer11
ENST00000587405.5:c.-95+2121del ENSP00000466478.1:n.-95+2121del
ENST00000587977.5:c.85del ENSP00000466587.1:p.Val29TrpfsTer11
ENST00000587982.5:n.191+2121del
ENST00000588372.5:c.-95+2121del ENSP00000468764.1:n.-95+2121del
ENST00000588594.5:c.85del ENSP00000465366.1:p.Val29TrpfsTer11
ENST00000589506.1:n.296del
ENST00000590016.5:c.85del ENSP00000466399.1:p.Val29TrpfsTer11
ENST00000590631.1:c.-111del ENSP00000465033.1:n.-111del
ENST00000591723.5:c.-134+2121del ENSP00000467986.1:n.-134+2121del
ENST00000592181.1:c.-154del ENSP00000464799.1:n.-154del
ENST00000592430.5:n.232+2121del
ENST00000592577.5:c.91del ENSP00000466839.1:p.Val31TrpfsTer11
ENST00000593039.5:c.3+2121del ENSP00000466834.1:n.3+2121del
NM_001142571.1:c.85del NP_001136043.1:p.Val29TrpfsTer11
NM_002878.3:c.85del , LRG_516t1:c.85del NP_002869.3:p.Val29TrpfsTer11
NM_133629.2:c.85del NP_598332.1:p.Val29TrpfsTer11
NR_037711.1:n.341del
NR_037712.1:n.341del
NR_037714.1:n.232+2121del
NM_001142571.2:c.85del NP_001136043.1:p.Val29TrpfsTer11
NM_133629.3:c.85del NP_598332.1:p.Val29TrpfsTer11
NR_037711.2:n.230del
NR_037712.2:n.230del
NM_002878.4:c.85del MANE Select NP_002869.3:p.Val29TrpfsTer11
Search 100 bp 5'
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