Canonical Allele Identifier: CA8499492

Gene: RAD51D

Linked Data

• ClinVar Variation Id: 239396
• ClinVar RCV Id: RCV000229969
• dbSNP Id: rs756059587
• ExAC: 17:33434149 T / C
• gnomAD v2: 17-33434149-T-C
• gnomAD v3: 17-35107130-T-C
• gnomAD v4: 17-35107130-T-C
• MyVariant Identifiers: chr17:g.33434149T>C (hg19) ; chr17:g.35107130T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35107130T>C , CM000679.2:g.35107130T>C	GRCh38
NC_000017.10:g.33434149T>C , CM000679.1:g.33434149T>C	GRCh37
NC_000017.9:g.30458262T>C	NCBI36
NG_031858.1:g.17740A>G , LRG_516:g.17740A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.345+236A>G	ENSP00000468273.3:n.345+236A>G
ENST00000587405.6:c.-12-8A>G	ENSP00000466478.2:n.-12-8A>G
ENST00000590016.6:c.406-8A>G	ENSP00000466399.1:n.406-8A>G
ENST00000590631.2:n.437-649A>G
ENST00000592577.6:c.-12-8A>G	ENSP00000466839.2:n.-12-8A>G
ENST00000345365.11:c.346-8A>G MANE Select	ENSP00000338790.6:n.346-8A>G
ENST00000335858.11:c.145-649A>G	ENSP00000338408.6:n.145-649A>G
ENST00000345365.10:c.346-8A>G	ENSP00000338790.6:n.346-8A>G
ENST00000394589.8:c.346-8A>G	ENSP00000378090.4:n.346-8A>G
ENST00000415064.6:n.496-8A>G
ENST00000460118.6:c.-125-69A>G	ENSP00000464356.2:n.-125-69A>G
ENST00000585343.5:c.428-8A>G
ENST00000585947.5:n.242-8A>G
ENST00000585982.5:n.500+236A>G
ENST00000586044.5:c.*77-8A>G	ENSP00000465584.1:n.*77-8A>G
ENST00000586186.2:c.248+236A>G
ENST00000586210.5:c.264-8A>G	ENSP00000465612.1:n.264-8A>G
ENST00000587405.5:c.-12-8A>G	ENSP00000466478.1:n.-12-8A>G
ENST00000587977.5:c.*86-8A>G	ENSP00000466587.1:n.*86-8A>G
ENST00000587982.5:n.273+236A>G
ENST00000588372.5:c.-12-8A>G	ENSP00000468764.1:n.-12-8A>G
ENST00000588594.5:c.*76+236A>G	ENSP00000465366.1:n.*76+236A>G
ENST00000590016.5:c.406-8A>G	ENSP00000466399.1:n.406-8A>G
ENST00000590631.1:c.-51-649A>G	ENSP00000465033.1:n.-51-649A>G
ENST00000591723.5:c.-52+236A>G	ENSP00000467986.1:n.-52+236A>G
ENST00000592181.1:c.-12-8A>G	ENSP00000464799.1:n.-12-8A>G
ENST00000592430.5:n.315-8A>G
ENST00000592577.5:c.352-8A>G	ENSP00000466839.1:n.352-8A>G
ENST00000592850.5:c.346-649A>G
ENST00000592928.2:n.167-649A>G
ENST00000593039.5:c.4-649A>G	ENSP00000466834.1:n.4-649A>G
NM_001142571.1:c.406-8A>G	NP_001136043.1:n.406-8A>G
NM_002878.3:c.346-8A>G , LRG_516t1:c.346-8A>G	NP_002869.3:n.346-8A>G
NM_133629.2:c.145-649A>G	NP_598332.1:n.145-649A>G
NR_037711.1:n.483-8A>G
NR_037712.1:n.482+236A>G
NR_037714.1:n.233-649A>G
NM_001142571.2:c.406-8A>G	NP_001136043.1:n.406-8A>G
NM_133629.3:c.145-649A>G	NP_598332.1:n.145-649A>G
NR_037711.2:n.372-8A>G
NR_037712.2:n.371+236A>G
NM_002878.4:c.346-8A>G MANE Select	NP_002869.3:n.346-8A>G