Canonical Allele Identifier: CA399089405

Gene: RAD51D

Linked Data

• dbSNP Id: rs786201358
• MyVariant Identifiers: chr17:g.33434138A>G (hg19) ; chr17:g.35107119A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35107119A>G , CM000679.2:g.35107119A>G	GRCh38
NC_000017.10:g.33434138A>G , CM000679.1:g.33434138A>G	GRCh37
NC_000017.9:g.30458251A>G	NCBI36
NG_031858.1:g.17751T>C , LRG_516:g.17751T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.345+247T>C	ENSP00000468273.3:n.345+247T>C
ENST00000587405.6:c.-9T>C	ENSP00000466478.2:n.-9T>C
ENST00000590016.6:c.409T>C	ENSP00000466399.1:p.Cys137Arg
ENST00000590631.2:n.437-638T>C
ENST00000592577.6:c.-9T>C	ENSP00000466839.2:n.-9T>C
ENST00000345365.11:c.349T>C MANE Select	ENSP00000338790.6:p.Cys117Arg
ENST00000335858.11:c.145-638T>C	ENSP00000338408.6:n.145-638T>C
ENST00000345365.10:c.349T>C	ENSP00000338790.6:p.Cys117Arg
ENST00000394589.8:c.349T>C	ENSP00000378090.4:p.Cys117Arg
ENST00000415064.6:n.499T>C
ENST00000460118.6:c.-125-58T>C	ENSP00000464356.2:n.-125-58T>C
ENST00000585343.5:c.431T>C
ENST00000585947.5:n.245T>C
ENST00000585982.5:n.500+247T>C
ENST00000586044.5:c.*80T>C	ENSP00000465584.1:n.*80T>C
ENST00000586186.2:c.248+247T>C
ENST00000586210.5:c.267T>C	ENSP00000465612.1:p.Tyr89=
ENST00000587405.5:c.-9T>C	ENSP00000466478.1:n.-9T>C
ENST00000587977.5:c.*89T>C	ENSP00000466587.1:n.*89T>C
ENST00000587982.5:n.273+247T>C
ENST00000588372.5:c.-9T>C	ENSP00000468764.1:n.-9T>C
ENST00000588594.5:c.*76+247T>C	ENSP00000465366.1:n.*76+247T>C
ENST00000590016.5:c.409T>C	ENSP00000466399.1:p.Cys137Arg
ENST00000590631.1:c.-51-638T>C	ENSP00000465033.1:n.-51-638T>C
ENST00000591723.5:c.-52+247T>C	ENSP00000467986.1:n.-52+247T>C
ENST00000592181.1:c.-9T>C	ENSP00000464799.1:n.-9T>C
ENST00000592430.5:n.318T>C
ENST00000592577.5:c.355T>C	ENSP00000466839.1:p.Cys119Arg
ENST00000592850.5:c.346-638T>C
ENST00000592928.2:n.167-638T>C
ENST00000593039.5:c.4-638T>C	ENSP00000466834.1:n.4-638T>C
NM_001142571.1:c.409T>C	NP_001136043.1:p.Cys137Arg
NM_002878.3:c.349T>C , LRG_516t1:c.349T>C	NP_002869.3:p.Cys117Arg
NM_133629.2:c.145-638T>C	NP_598332.1:n.145-638T>C
NR_037711.1:n.486T>C
NR_037712.1:n.482+247T>C
NR_037714.1:n.233-638T>C
NM_001142571.2:c.409T>C	NP_001136043.1:p.Cys137Arg
NM_133629.3:c.145-638T>C	NP_598332.1:n.145-638T>C
NR_037711.2:n.375T>C
NR_037712.2:n.371+247T>C
NM_002878.4:c.349T>C MANE Select	NP_002869.3:p.Cys117Arg