Canonical Allele Identifier: CA16620396

Gene: RAD51D

Linked Data

• ClinVar Variation Id: 420660
• ClinVar RCV Id: RCV001865452 ; RCV002436538 ; RCV003482146
• dbSNP Id: rs1064794619
• gnomAD v4: 17-35119612-A-C
• MyVariant Identifiers: chr17:g.33446631A>C (hg19) ; chr17:g.35119612A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35119612A>C , CM000679.2:g.35119612A>C	GRCh38
NC_000017.10:g.33446631A>C , CM000679.1:g.33446631A>C	GRCh37
NC_000017.9:g.30470744A>C	NCBI36
NG_031858.1:g.5258T>G , LRG_516:g.5258T>G
NG_054719.1:g.3034A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000586186.3:c.2T>G	ENSP00000468273.3:p.Met1Arg
ENST00000587405.6:c.-95+1679T>G	ENSP00000466478.2:n.-95+1679T>G
ENST00000590016.6:c.2T>G	ENSP00000466399.1:p.Met1Arg
ENST00000592577.6:c.-276+88T>G	ENSP00000466839.2:n.-276+88T>G
ENST00000345365.11:c.2T>G MANE Select	ENSP00000338790.6:p.Met1Arg
ENST00000335858.11:c.2T>G	ENSP00000338408.6:p.Met1Arg
ENST00000345365.10:c.2T>G	ENSP00000338790.6:p.Met1Arg
ENST00000394589.8:c.2T>G	ENSP00000378090.4:p.Met1Arg
ENST00000415064.6:n.233-440T>G
ENST00000460118.6:c.-350T>G	ENSP00000464356.2:n.-350T>G
ENST00000585947.5:n.159+1679T>G
ENST00000585982.5:n.178-440T>G
ENST00000586044.5:c.2T>G	ENSP00000465584.1:p.Met1Arg
ENST00000586210.5:c.2T>G	ENSP00000465612.1:p.Met1Arg
ENST00000587405.5:c.-95+1679T>G	ENSP00000466478.1:n.-95+1679T>G
ENST00000587977.5:c.2T>G	ENSP00000466587.1:p.Met1Arg
ENST00000587982.5:n.191+1679T>G
ENST00000588372.5:c.-95+1679T>G	ENSP00000468764.1:n.-95+1679T>G
ENST00000588594.5:c.2T>G	ENSP00000465366.1:p.Met1Arg
ENST00000589506.1:n.213T>G
ENST00000590016.5:c.2T>G	ENSP00000466399.1:p.Met1Arg
ENST00000591723.5:c.-134+1679T>G	ENSP00000467986.1:n.-134+1679T>G
ENST00000592181.1:c.-157+435T>G	ENSP00000464799.1:n.-157+435T>G
ENST00000592430.5:n.232+1679T>G
ENST00000592577.5:c.88+88T>G	ENSP00000466839.1:n.88+88T>G
ENST00000593039.5:c.3+1679T>G	ENSP00000466834.1:n.3+1679T>G
NM_001142571.1:c.2T>G	NP_001136043.1:p.Met1Arg
NM_002878.3:c.2T>G , LRG_516t1:c.2T>G	NP_002869.3:p.Met1Arg
NM_133629.2:c.2T>G	NP_598332.1:p.Met1Arg
NR_037711.1:n.258T>G
NR_037712.1:n.258T>G
NR_037714.1:n.232+1679T>G
NM_001142571.2:c.2T>G	NP_001136043.1:p.Met1Arg
NM_133629.3:c.2T>G	NP_598332.1:p.Met1Arg
NR_037711.2:n.147T>G
NR_037712.2:n.147T>G
NM_002878.4:c.2T>G MANE Select	NP_002869.3:p.Met1Arg