Canonical Allele Identifier: CA499731558

Gene: RAD51D

Linked Data

• ClinVar Variation Id: 794648
• ClinVar RCV Id: RCV003372926
• dbSNP Id: rs1597861626
• gnomAD v4: 17-35106389-C-T
• MyVariant Identifiers: chr17:g.33433408C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35106389C>T , CM000679.2:g.35106389C>T	GRCh38
NC_000017.10:g.33433408C>T , CM000679.1:g.33433408C>T	GRCh37
NC_000017.9:g.30457521C>T	NCBI36
NG_031858.1:g.18481G>A , LRG_516:g.18481G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000586186.3:c.438G>A	ENSP00000468273.3:p.Gln146=
ENST00000587405.6:c.216G>A	ENSP00000466478.2:p.Gln72=
ENST00000590016.6:c.633G>A	ENSP00000466399.1:p.Gln211=
ENST00000590631.2:n.529G>A
ENST00000592577.6:c.216G>A	ENSP00000466839.2:p.Gln72=
ENST00000345365.11:c.573G>A MANE Select	ENSP00000338790.6:p.Gln191=
ENST00000335858.11:c.237G>A	ENSP00000338408.6:p.Gln79=
ENST00000345365.10:c.573G>A	ENSP00000338790.6:p.Gln191=
ENST00000394589.8:c.573G>A	ENSP00000378090.4:p.Gln191=
ENST00000415064.6:n.723G>A
ENST00000460118.6:c.42G>A	ENSP00000464356.2:p.Gln14=
ENST00000585947.5:n.469G>A
ENST00000585982.5:n.593G>A
ENST00000586044.5:c.*304G>A	ENSP00000465584.1:n.*304G>A
ENST00000586210.5:c.*167G>A	ENSP00000465612.1:n.*167G>A
ENST00000587405.5:c.216G>A	ENSP00000466478.1:p.Gln72=
ENST00000587977.5:c.*313G>A	ENSP00000466587.1:n.*313G>A
ENST00000587982.5:n.366G>A
ENST00000588372.5:c.216G>A	ENSP00000468764.1:p.Gln72=
ENST00000588594.5:c.*169G>A	ENSP00000465366.1:n.*169G>A
ENST00000590016.5:c.633G>A	ENSP00000466399.1:p.Gln211=
ENST00000590631.1:c.42G>A	ENSP00000465033.1:p.Gln14=
ENST00000591723.5:c.42G>A	ENSP00000467986.1:p.Gln14=
ENST00000592181.1:c.216G>A	ENSP00000464799.1:p.Gln72=
ENST00000592430.5:n.542G>A
ENST00000592577.5:c.579G>A	ENSP00000466839.1:p.Gln193=
ENST00000593039.5:c.96G>A	ENSP00000466834.1:p.Gln32=
NM_001142571.1:c.633G>A	NP_001136043.1:p.Gln211=
NM_002878.3:c.573G>A , LRG_516t1:c.573G>A	NP_002869.3:p.Gln191=
NM_133629.2:c.237G>A	NP_598332.1:p.Gln79=
NR_037711.1:n.710G>A
NR_037712.1:n.575G>A
NR_037714.1:n.325G>A
NM_001142571.2:c.633G>A	NP_001136043.1:p.Gln211=
NM_133629.3:c.237G>A	NP_598332.1:p.Gln79=
NR_037711.2:n.599G>A
NR_037712.2:n.464G>A
NM_002878.4:c.573G>A MANE Select	NP_002869.3:p.Gln191=