Canonical Allele Identifier: CA499731862

Gene: RAD51D

Linked Data

• ClinVar Variation Id: 492426
• ClinVar RCV Id: RCV000583256 ; RCV003483683 ; RCV004024644
• dbSNP Id: rs1555568469
• MyVariant Identifiers: chr17:g.33434385C>T (hg19) ; chr17:g.35107366C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35107366C>T , CM000679.2:g.35107366C>T	GRCh38
NC_000017.10:g.33434385C>T , CM000679.1:g.33434385C>T	GRCh37
NC_000017.9:g.30458498C>T	NCBI36
NG_031858.1:g.17504G>A , LRG_516:g.17504G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.345G>A	ENSP00000468273.3:p.Gln115=
ENST00000587405.6:c.-13G>A	ENSP00000466478.2:n.-13G>A
ENST00000590016.6:c.405G>A	ENSP00000466399.1:p.Gln135=
ENST00000590631.2:n.437-885G>A
ENST00000592577.6:c.-13G>A	ENSP00000466839.2:n.-13G>A
ENST00000345365.11:c.345G>A MANE Select	ENSP00000338790.6:p.Gln115=
ENST00000335858.11:c.145-885G>A	ENSP00000338408.6:n.145-885G>A
ENST00000345365.10:c.345G>A	ENSP00000338790.6:p.Gln115=
ENST00000394589.8:c.345G>A	ENSP00000378090.4:p.Gln115=
ENST00000415064.6:n.495G>A
ENST00000460118.6:c.-126G>A	ENSP00000464356.2:n.-126G>A
ENST00000585343.5:c.427G>A
ENST00000585947.5:n.241G>A
ENST00000585982.5:n.500G>A
ENST00000586044.5:c.*76G>A	ENSP00000465584.1:n.*76G>A
ENST00000586186.2:c.248G>A
ENST00000586210.5:c.264-244G>A	ENSP00000465612.1:n.264-244G>A
ENST00000587405.5:c.-13G>A	ENSP00000466478.1:n.-13G>A
ENST00000587977.5:c.*86-244G>A	ENSP00000466587.1:n.*86-244G>A
ENST00000587982.5:n.273G>A
ENST00000588372.5:c.-13G>A	ENSP00000468764.1:n.-13G>A
ENST00000588594.5:c.*76G>A	ENSP00000465366.1:n.*76G>A
ENST00000589506.1:n.437G>A
ENST00000590016.5:c.405G>A	ENSP00000466399.1:p.Gln135=
ENST00000590631.1:c.-51-885G>A	ENSP00000465033.1:n.-51-885G>A
ENST00000591723.5:c.-52G>A	ENSP00000467986.1:n.-52G>A
ENST00000592181.1:c.-13G>A	ENSP00000464799.1:n.-13G>A
ENST00000592430.5:n.314G>A
ENST00000592577.5:c.351G>A	ENSP00000466839.1:p.Gln117=
ENST00000592850.5:c.346-885G>A
ENST00000592928.2:n.167-885G>A
ENST00000593039.5:c.4-885G>A	ENSP00000466834.1:n.4-885G>A
NM_001142571.1:c.405G>A	NP_001136043.1:p.Gln135=
NM_002878.3:c.345G>A , LRG_516t1:c.345G>A	NP_002869.3:p.Gln115=
NM_133629.2:c.145-885G>A	NP_598332.1:n.145-885G>A
NR_037711.1:n.482G>A
NR_037712.1:n.482G>A
NR_037714.1:n.233-885G>A
NM_001142571.2:c.405G>A	NP_001136043.1:p.Gln135=
NM_133629.3:c.145-885G>A	NP_598332.1:n.145-885G>A
NR_037711.2:n.371G>A
NR_037712.2:n.371G>A
NM_002878.4:c.345G>A MANE Select	NP_002869.3:p.Gln115=