Canonical Allele Identifier: CA10580439

Gene: RAD51D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35100996C>A , CM000679.2:g.35100996C>A	GRCh38
NC_000017.10:g.33428015C>A , CM000679.1:g.33428015C>A	GRCh37
NC_000017.9:g.30452128C>A	NCBI36
NG_031858.1:g.23874G>T , LRG_516:g.23874G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.809G>T	ENSP00000468273.3:p.Gly270Val
ENST00000587405.6:c.587G>T	ENSP00000466478.2:p.Gly196Val
ENST00000590016.6:c.1004G>T	ENSP00000466399.1:p.Gly335Val
ENST00000592577.6:c.587G>T	ENSP00000466839.2:p.Gly196Val
ENST00000345365.11:c.944G>T MANE Select	ENSP00000338790.6:p.Gly315Val
ENST00000335858.11:c.608G>T	ENSP00000338408.6:p.Gly203Val
ENST00000345365.10:c.944G>T	ENSP00000338790.6:p.Gly315Val
ENST00000394589.8:c.944G>T	ENSP00000378090.4:p.Gly315Val
ENST00000460118.6:c.413G>T	ENSP00000464356.2:p.Gly138Val
ENST00000586044.5:c.*675G>T	ENSP00000465584.1:n.*675G>T
ENST00000586210.5:c.*538G>T	ENSP00000465612.1:n.*538G>T
ENST00000587977.5:c.*684G>T	ENSP00000466587.1:n.*684G>T
ENST00000588372.5:c.*427G>T	ENSP00000468764.1:n.*427G>T
ENST00000588594.5:c.*540G>T	ENSP00000465366.1:n.*540G>T
ENST00000590016.5:c.1004G>T	ENSP00000466399.1:p.Gly335Val
ENST00000591723.5:c.372+205G>T	ENSP00000467986.1:n.372+205G>T
ENST00000592181.1:c.546+205G>T	ENSP00000464799.1:n.546+205G>T
ENST00000593039.5:c.426+205G>T	ENSP00000466834.1:n.426+205G>T
NM_001142571.1:c.1004G>T	NP_001136043.1:p.Gly335Val
NM_002878.3:c.944G>T , LRG_516t1:c.944G>T	NP_002869.3:p.Gly315Val
NM_133629.2:c.608G>T	NP_598332.1:p.Gly203Val
NR_037711.1:n.1081G>T
NR_037712.1:n.946G>T
NR_037714.1:n.655+205G>T
NM_001142571.2:c.1004G>T	NP_001136043.1:p.Gly335Val
NM_133629.3:c.608G>T	NP_598332.1:p.Gly203Val
NR_037711.2:n.970G>T
NR_037712.2:n.835G>T
NM_002878.4:c.944G>T MANE Select	NP_002869.3:p.Gly315Val