Canonical Allele Identifier: CA293036

Gene: RAD51D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35101231G>A , CM000679.2:g.35101231G>A	GRCh38
NC_000017.10:g.33428250G>A , CM000679.1:g.33428250G>A	GRCh37
NC_000017.9:g.30452363G>A	NCBI36
NG_031858.1:g.23639C>T , LRG_516:g.23639C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.738C>T	ENSP00000468273.3:p.Arg246=
ENST00000587405.6:c.516C>T	ENSP00000466478.2:p.Arg172=
ENST00000590016.6:c.933C>T	ENSP00000466399.1:p.Arg311=
ENST00000592577.6:c.516C>T	ENSP00000466839.2:p.Arg172=
ENST00000345365.11:c.873C>T MANE Select	ENSP00000338790.6:p.Arg291=
ENST00000335858.11:c.537C>T	ENSP00000338408.6:p.Arg179=
ENST00000345365.10:c.873C>T	ENSP00000338790.6:p.Arg291=
ENST00000394589.8:c.873C>T	ENSP00000378090.4:p.Arg291=
ENST00000460118.6:c.342C>T	ENSP00000464356.2:p.Arg114=
ENST00000586044.5:c.*604C>T	ENSP00000465584.1:n.*604C>T
ENST00000586210.5:c.*467C>T	ENSP00000465612.1:n.*467C>T
ENST00000587977.5:c.*613C>T	ENSP00000466587.1:n.*613C>T
ENST00000588372.5:c.*356C>T	ENSP00000468764.1:n.*356C>T
ENST00000588594.5:c.*469C>T	ENSP00000465366.1:n.*469C>T
ENST00000590016.5:c.933C>T	ENSP00000466399.1:p.Arg311=
ENST00000591723.5:c.342C>T	ENSP00000467986.1:p.Arg114=
ENST00000592181.1:c.516C>T	ENSP00000464799.1:p.Arg172=
ENST00000593039.5:c.396C>T	ENSP00000466834.1:p.Arg132=
NM_001142571.1:c.933C>T	NP_001136043.1:p.Arg311=
NM_002878.3:c.873C>T , LRG_516t1:c.873C>T	NP_002869.3:p.Arg291=
NM_133629.2:c.537C>T	NP_598332.1:p.Arg179=
NR_037711.1:n.1010C>T
NR_037712.1:n.875C>T
NR_037714.1:n.625C>T
NM_001142571.2:c.933C>T	NP_001136043.1:p.Arg311=
NM_133629.3:c.537C>T	NP_598332.1:p.Arg179=
NR_037711.2:n.899C>T
NR_037712.2:n.764C>T
NM_002878.4:c.873C>T MANE Select	NP_002869.3:p.Arg291=