Canonical Allele Identifier: CA2257361542

Gene: RAD51D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35106394C= , CM000679.2:g.35106394C=	GRCh38
NC_000017.10:g.33433413C= , CM000679.1:g.33433413C=	GRCh37
NC_000017.9:g.30457526C=	NCBI36
NG_031858.1:g.18476G= , LRG_516:g.18476G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000586186.3:c.433G=	ENSP00000468273.3:p.Ala145=
ENST00000587405.6:c.211G=	ENSP00000466478.2:p.Ala71=
ENST00000590016.6:c.628G=	ENSP00000466399.1:p.Ala210=
ENST00000590631.2:n.524G=
ENST00000592577.6:c.211G=	ENSP00000466839.2:p.Ala71=
ENST00000345365.11:c.568G= MANE Select	ENSP00000338790.6:p.Ala190=
ENST00000335858.11:c.232G=	ENSP00000338408.6:p.Ala78=
ENST00000345365.10:c.568G=	ENSP00000338790.6:p.Ala190=
ENST00000394589.8:c.568G=	ENSP00000378090.4:p.Ala190=
ENST00000415064.6:n.718G=
ENST00000460118.6:c.37G=	ENSP00000464356.2:p.Ala13=
ENST00000585947.5:n.464G=
ENST00000585982.5:n.588G=
ENST00000586044.5:c.*299G=	ENSP00000465584.1:n.*299G=
ENST00000586210.5:c.*162G=	ENSP00000465612.1:n.*162G=
ENST00000587405.5:c.211G=	ENSP00000466478.1:p.Ala71=
ENST00000587977.5:c.*308G=	ENSP00000466587.1:n.*308G=
ENST00000587982.5:n.361G=
ENST00000588372.5:c.211G=	ENSP00000468764.1:p.Ala71=
ENST00000588594.5:c.*164G=	ENSP00000465366.1:n.*164G=
ENST00000590016.5:c.628G=	ENSP00000466399.1:p.Ala210=
ENST00000590631.1:c.37G=	ENSP00000465033.1:p.Ala13=
ENST00000591723.5:c.37G=	ENSP00000467986.1:p.Ala13=
ENST00000592181.1:c.211G=	ENSP00000464799.1:p.Ala71=
ENST00000592430.5:n.537G=
ENST00000592577.5:c.574G=	ENSP00000466839.1:p.Ala192=
ENST00000593039.5:c.91G=	ENSP00000466834.1:p.Ala31=
NM_001142571.1:c.628G=	NP_001136043.1:p.Ala210=
NM_002878.3:c.568G= , LRG_516t1:c.568G=	NP_002869.3:p.Ala190=
NM_133629.2:c.232G=	NP_598332.1:p.Ala78=
NR_037711.1:n.705G=
NR_037712.1:n.570G=
NR_037714.1:n.320G=
NM_001142571.2:c.628G=	NP_001136043.1:p.Ala210=
NM_133629.3:c.232G=	NP_598332.1:p.Ala78=
NR_037711.2:n.594G=
NR_037712.2:n.459G=
NM_002878.4:c.568G= MANE Select	NP_002869.3:p.Ala190=