Canonical Allele Identifier: CA399086029

Gene: RAD51D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35100958T>A , CM000679.2:g.35100958T>A	GRCh38
NC_000017.10:g.33427977T>A , CM000679.1:g.33427977T>A	GRCh37
NC_000017.9:g.30452090T>A	NCBI36
NG_031858.1:g.23912A>T , LRG_516:g.23912A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.847A>T	ENSP00000468273.3:p.Thr283Ser
ENST00000587405.6:c.625A>T	ENSP00000466478.2:p.Thr209Ser
ENST00000590016.6:c.1042A>T	ENSP00000466399.1:p.Thr348Ser
ENST00000592577.6:c.625A>T	ENSP00000466839.2:p.Thr209Ser
ENST00000345365.11:c.982A>T MANE Select	ENSP00000338790.6:p.Thr328Ser
ENST00000335858.11:c.646A>T	ENSP00000338408.6:p.Thr216Ser
ENST00000345365.10:c.982A>T	ENSP00000338790.6:p.Thr328Ser
ENST00000394589.8:c.982A>T	ENSP00000378090.4:p.Thr328Ser
ENST00000460118.6:c.451A>T	ENSP00000464356.2:p.Thr151Ser
ENST00000586044.5:c.*713A>T	ENSP00000465584.1:n.*713A>T
ENST00000586210.5:c.*576A>T	ENSP00000465612.1:n.*576A>T
ENST00000587977.5:c.*722A>T	ENSP00000466587.1:n.*722A>T
ENST00000588372.5:c.*465A>T	ENSP00000468764.1:n.*465A>T
ENST00000588594.5:c.*578A>T	ENSP00000465366.1:n.*578A>T
ENST00000590016.5:c.1042A>T	ENSP00000466399.1:p.Thr348Ser
ENST00000591723.5:c.372+243A>T	ENSP00000467986.1:n.372+243A>T
ENST00000592181.1:c.546+243A>T	ENSP00000464799.1:n.546+243A>T
ENST00000593039.5:c.426+243A>T	ENSP00000466834.1:n.426+243A>T
NM_001142571.1:c.1042A>T	NP_001136043.1:p.Thr348Ser
NM_002878.3:c.982A>T , LRG_516t1:c.982A>T	NP_002869.3:p.Thr328Ser
NM_133629.2:c.646A>T	NP_598332.1:p.Thr216Ser
NR_037711.1:n.1119A>T
NR_037712.1:n.984A>T
NR_037714.1:n.655+243A>T
NM_001142571.2:c.1042A>T	NP_001136043.1:p.Thr348Ser
NM_133629.3:c.646A>T	NP_598332.1:p.Thr216Ser
NR_037711.2:n.1008A>T
NR_037712.2:n.873A>T
NM_002878.4:c.982A>T MANE Select	NP_002869.3:p.Thr328Ser