Canonical Allele Identifier: CA2257352351

Gene: RAD51D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35119613T= , CM000679.2:g.35119613T=	GRCh38
NC_000017.10:g.33446632T= , CM000679.1:g.33446632T=	GRCh37
NC_000017.9:g.30470745T=	NCBI36
NG_031858.1:g.5257A= , LRG_516:g.5257A=
NG_054719.1:g.3035T=

Transcript Alleles

HGVS	Amino-acid Change
NM_002878.4:c.1A= MANE Select	NP_002869.3:p.Met1=
ENST00000345365.11:c.1A= MANE Select	ENSP00000338790.6:p.Met1=
NM_001142571.1:c.1A=	NP_001136043.1:p.Met1=
NM_001142571.2:c.1A=	NP_001136043.1:p.Met1=
NM_002878.3:c.1A= , LRG_516t1:c.1A=	NP_002869.3:p.Met1=
NM_133629.2:c.1A=	NP_598332.1:p.Met1=
NM_133629.3:c.1A=	NP_598332.1:p.Met1=
NR_037711.1:n.257A=
NR_037711.2:n.146A=
NR_037712.1:n.257A=
NR_037712.2:n.146A=
NR_037714.1:n.232+1678A=
ENST00000335858.11:c.1A=	ENSP00000338408.6:p.Met1=
ENST00000345365.10:c.1A=	ENSP00000338790.6:p.Met1=
ENST00000394589.8:c.1A=	ENSP00000378090.4:p.Met1=
ENST00000415064.6:n.233-441A=
ENST00000460118.6:c.-351A=	ENSP00000464356.2:n.-351A=
ENST00000585947.5:n.159+1678A=
ENST00000585982.5:n.178-441A=
ENST00000586044.5:c.1A=	ENSP00000465584.1:p.Met1=
ENST00000586186.3:c.1A=	ENSP00000468273.3:p.Met1=
ENST00000586210.5:c.1A=	ENSP00000465612.1:p.Met1=
ENST00000587405.5:c.-95+1678A=	ENSP00000466478.1:n.-95+1678A=
ENST00000587405.6:c.-95+1678A=	ENSP00000466478.2:n.-95+1678A=
ENST00000587977.5:c.1A=	ENSP00000466587.1:p.Met1=
ENST00000587982.5:n.191+1678A=
ENST00000588372.5:c.-95+1678A=	ENSP00000468764.1:n.-95+1678A=
ENST00000588594.5:c.1A=	ENSP00000465366.1:p.Met1=
ENST00000589506.1:n.212A=
ENST00000590016.5:c.1A=	ENSP00000466399.1:p.Met1=
ENST00000590016.6:c.1A=	ENSP00000466399.1:p.Met1=
ENST00000591723.5:c.-134+1678A=	ENSP00000467986.1:n.-134+1678A=
ENST00000592181.1:c.-157+434A=	ENSP00000464799.1:n.-157+434A=
ENST00000592430.5:n.232+1678A=
ENST00000592577.5:c.88+87A=	ENSP00000466839.1:n.88+87A=
ENST00000592577.6:c.-276+87A=	ENSP00000466839.2:n.-276+87A=
ENST00000593039.5:c.3+1678A=	ENSP00000466834.1:n.3+1678A=