Canonical Allele Identifier: CA2257360279

Gene: RAD51D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35103393A= , CM000679.2:g.35103393A=	GRCh38
NC_000017.10:g.33430412A= , CM000679.1:g.33430412A=	GRCh37
NC_000017.9:g.30454525A=	NCBI36
NG_031858.1:g.21477T= , LRG_516:g.21477T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.532+61T=	ENSP00000468273.3:n.532+61T=
ENST00000587405.6:c.310+61T=	ENSP00000466478.2:n.310+61T=
ENST00000590016.6:c.727+61T=	ENSP00000466399.1:n.727+61T=
ENST00000592577.6:c.310+61T=	ENSP00000466839.2:n.310+61T=
ENST00000345365.11:c.667+61T= MANE Select	ENSP00000338790.6:n.667+61T=
ENST00000335858.11:c.331+61T=	ENSP00000338408.6:n.331+61T=
ENST00000345365.10:c.667+61T=	ENSP00000338790.6:n.667+61T=
ENST00000394589.8:c.667+61T=	ENSP00000378090.4:n.667+61T=
ENST00000460118.6:c.136+61T=	ENSP00000464356.2:n.136+61T=
ENST00000586044.5:c.*398+61T=	ENSP00000465584.1:n.*398+61T=
ENST00000586210.5:c.*261+61T=	ENSP00000465612.1:n.*261+61T=
ENST00000587405.5:c.310+61T=	ENSP00000466478.1:n.310+61T=
ENST00000587977.5:c.*407+61T=	ENSP00000466587.1:n.*407+61T=
ENST00000588372.5:c.*150+61T=	ENSP00000468764.1:n.*150+61T=
ENST00000588594.5:c.*263+61T=	ENSP00000465366.1:n.*263+61T=
ENST00000590016.5:c.727+61T=	ENSP00000466399.1:n.727+61T=
ENST00000591723.5:c.136+61T=	ENSP00000467986.1:n.136+61T=
ENST00000592181.1:c.310+61T=	ENSP00000464799.1:n.310+61T=
ENST00000592577.5:c.673+61T=	ENSP00000466839.1:n.673+61T=
ENST00000593039.5:c.190+61T=	ENSP00000466834.1:n.190+61T=
NM_001142571.1:c.727+61T=	NP_001136043.1:n.727+61T=
NM_002878.3:c.667+61T= , LRG_516t1:c.667+61T=	NP_002869.3:n.667+61T=
NM_133629.2:c.331+61T=	NP_598332.1:n.331+61T=
NR_037711.1:n.804+61T=
NR_037712.1:n.669+61T=
NR_037714.1:n.419+61T=
NM_001142571.2:c.727+61T=	NP_001136043.1:n.727+61T=
NM_133629.3:c.331+61T=	NP_598332.1:n.331+61T=
NR_037711.2:n.693+61T=
NR_037712.2:n.558+61T=
NM_002878.4:c.667+61T= MANE Select	NP_002869.3:n.667+61T=