Canonical Allele Identifier: CA129085

Gene: RAD51D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35101347G>A , CM000679.2:g.35101347G>A	GRCh38
NC_000017.10:g.33428366G>A , CM000679.1:g.33428366G>A	GRCh37
NC_000017.9:g.30452479G>A	NCBI36
NG_031858.1:g.23523C>T , LRG_516:g.23523C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002878.4:c.757C>T MANE Select	NP_002869.3:p.Arg253Ter
ENST00000345365.11:c.757C>T MANE Select	ENSP00000338790.6:p.Arg253Ter
NM_001142571.1:c.817C>T	NP_001136043.1:p.Arg273Ter
NM_001142571.2:c.817C>T	NP_001136043.1:p.Arg273Ter
NM_002878.3:c.757C>T , LRG_516t1:c.757C>T	NP_002869.3:p.Arg253Ter
NM_133629.2:c.421C>T	NP_598332.1:p.Arg141Ter
NM_133629.3:c.421C>T	NP_598332.1:p.Arg141Ter
NR_037711.1:n.894C>T
NR_037711.2:n.783C>T
NR_037712.1:n.759C>T
NR_037712.2:n.648C>T
NR_037714.1:n.509C>T
ENST00000335858.11:c.421C>T	ENSP00000338408.6:p.Arg141Ter
ENST00000345365.10:c.757C>T	ENSP00000338790.6:p.Arg253Ter
ENST00000394589.8:c.757C>T	ENSP00000378090.4:p.Arg253Ter
ENST00000460118.6:c.226C>T	ENSP00000464356.2:p.Arg76Ter
ENST00000586044.5:c.*488C>T	ENSP00000465584.1:n.*488C>T
ENST00000586186.3:c.622C>T	ENSP00000468273.3:p.Arg208Ter
ENST00000586210.5:c.*351C>T	ENSP00000465612.1:n.*351C>T
ENST00000587405.5:c.400C>T	ENSP00000466478.1:p.Arg134Ter
ENST00000587405.6:c.400C>T	ENSP00000466478.2:p.Arg134Ter
ENST00000587977.5:c.*497C>T	ENSP00000466587.1:n.*497C>T
ENST00000588372.5:c.*240C>T	ENSP00000468764.1:n.*240C>T
ENST00000588594.5:c.*353C>T	ENSP00000465366.1:n.*353C>T
ENST00000590016.5:c.817C>T	ENSP00000466399.1:p.Arg273Ter
ENST00000590016.6:c.817C>T	ENSP00000466399.1:p.Arg273Ter
ENST00000591723.5:c.226C>T	ENSP00000467986.1:p.Arg76Ter
ENST00000592181.1:c.400C>T	ENSP00000464799.1:p.Arg134Ter
ENST00000592577.6:c.400C>T	ENSP00000466839.2:p.Arg134Ter
ENST00000593039.5:c.280C>T	ENSP00000466834.1:p.Arg94Ter