Canonical Allele Identifier: CA8499485

Gene: RAD51D

Linked Data

• ClinVar Variation Id: 641939
• ClinVar RCV Id: RCV000795299 ; RCV002345752
• dbSNP Id: rs144603589
• ExAC: 17:33434110 T / C
• gnomAD v4: 17-35107091-T-C
• MyVariant Identifiers: chr17:g.33434110T>C (hg19) ; chr17:g.35107091T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35107091T>C , CM000679.2:g.35107091T>C	GRCh38
NC_000017.10:g.33434110T>C , CM000679.1:g.33434110T>C	GRCh37
NC_000017.9:g.30458223T>C	NCBI36
NG_031858.1:g.17779A>G , LRG_516:g.17779A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.345+275A>G	ENSP00000468273.3:n.345+275A>G
ENST00000587405.6:c.20A>G	ENSP00000466478.2:p.His7Arg
ENST00000590016.6:c.437A>G	ENSP00000466399.1:p.His146Arg
ENST00000590631.2:n.437-610A>G
ENST00000592577.6:c.20A>G	ENSP00000466839.2:p.His7Arg
ENST00000345365.11:c.377A>G MANE Select	ENSP00000338790.6:p.His126Arg
ENST00000335858.11:c.145-610A>G	ENSP00000338408.6:n.145-610A>G
ENST00000345365.10:c.377A>G	ENSP00000338790.6:p.His126Arg
ENST00000394589.8:c.377A>G	ENSP00000378090.4:p.His126Arg
ENST00000415064.6:n.527A>G
ENST00000460118.6:c.-125-30A>G	ENSP00000464356.2:n.-125-30A>G
ENST00000585343.5:c.459A>G
ENST00000585947.5:n.273A>G
ENST00000585982.5:n.500+275A>G
ENST00000586044.5:c.*108A>G	ENSP00000465584.1:n.*108A>G
ENST00000586186.2:c.248+275A>G
ENST00000586210.5:c.295A>G	ENSP00000465612.1:p.Met99Val
ENST00000587405.5:c.20A>G	ENSP00000466478.1:p.His7Arg
ENST00000587977.5:c.*117A>G	ENSP00000466587.1:n.*117A>G
ENST00000587982.5:n.273+275A>G
ENST00000588372.5:c.20A>G	ENSP00000468764.1:p.His7Arg
ENST00000588594.5:c.*76+275A>G	ENSP00000465366.1:n.*76+275A>G
ENST00000590016.5:c.437A>G	ENSP00000466399.1:p.His146Arg
ENST00000590631.1:c.-51-610A>G	ENSP00000465033.1:n.-51-610A>G
ENST00000591723.5:c.-52+275A>G	ENSP00000467986.1:n.-52+275A>G
ENST00000592181.1:c.20A>G	ENSP00000464799.1:p.His7Arg
ENST00000592430.5:n.346A>G
ENST00000592577.5:c.383A>G	ENSP00000466839.1:p.His128Arg
ENST00000592850.5:c.346-610A>G
ENST00000592928.2:n.167-610A>G
ENST00000593039.5:c.4-610A>G	ENSP00000466834.1:n.4-610A>G
NM_001142571.1:c.437A>G	NP_001136043.1:p.His146Arg
NM_002878.3:c.377A>G , LRG_516t1:c.377A>G	NP_002869.3:p.His126Arg
NM_133629.2:c.145-610A>G	NP_598332.1:n.145-610A>G
NR_037711.1:n.514A>G
NR_037712.1:n.482+275A>G
NR_037714.1:n.233-610A>G
NM_001142571.2:c.437A>G	NP_001136043.1:p.His146Arg
NM_133629.3:c.145-610A>G	NP_598332.1:n.145-610A>G
NR_037711.2:n.403A>G
NR_037712.2:n.371+275A>G
NM_002878.4:c.377A>G MANE Select	NP_002869.3:p.His126Arg