Canonical Allele Identifier: CA16620392

Gene: RAD51D

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35119533del , CM000679.2:g.35119533del	GRCh38
NC_000017.10:g.33446552del , CM000679.1:g.33446552del	GRCh37
NC_000017.9:g.30470665del	NCBI36
NG_031858.1:g.5337del , LRG_516:g.5337del
NG_054719.1:g.2955del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.81del	ENSP00000468273.3:p.Val28TrpfsTer12
ENST00000587405.6:c.-95+1758del	ENSP00000466478.2:n.-95+1758del
ENST00000590016.6:c.81del	ENSP00000466399.1:p.Val28TrpfsTer12
ENST00000590631.2:n.14del
ENST00000592577.6:c.-276+167del	ENSP00000466839.2:n.-276+167del
ENST00000345365.11:c.81del MANE Select	ENSP00000338790.6:p.Val28TrpfsTer12
ENST00000335858.11:c.81del	ENSP00000338408.6:p.Val28TrpfsTer12
ENST00000345365.10:c.81del	ENSP00000338790.6:p.Val28TrpfsTer12
ENST00000394589.8:c.81del	ENSP00000378090.4:p.Val28TrpfsTer12
ENST00000415064.6:n.233-361del
ENST00000460118.6:c.-271del	ENSP00000464356.2:n.-271del
ENST00000585947.5:n.159+1758del
ENST00000585982.5:n.178-361del
ENST00000586044.5:c.81del	ENSP00000465584.1:p.Val28TrpfsTer12
ENST00000586210.5:c.81del	ENSP00000465612.1:p.Val28TrpfsTer12
ENST00000587405.5:c.-95+1758del	ENSP00000466478.1:n.-95+1758del
ENST00000587977.5:c.81del	ENSP00000466587.1:p.Val28TrpfsTer12
ENST00000587982.5:n.191+1758del
ENST00000588372.5:c.-95+1758del	ENSP00000468764.1:n.-95+1758del
ENST00000588594.5:c.81del	ENSP00000465366.1:p.Val28TrpfsTer12
ENST00000589506.1:n.292del
ENST00000590016.5:c.81del	ENSP00000466399.1:p.Val28TrpfsTer12
ENST00000590631.1:c.-474del	ENSP00000465033.1:n.-474del
ENST00000591723.5:c.-134+1758del	ENSP00000467986.1:n.-134+1758del
ENST00000592181.1:c.-156-361del	ENSP00000464799.1:n.-156-361del
ENST00000592430.5:n.232+1758del
ENST00000592577.5:c.88+167del	ENSP00000466839.1:n.88+167del
ENST00000593039.5:c.3+1758del	ENSP00000466834.1:n.3+1758del
NM_001142571.1:c.81del	NP_001136043.1:p.Val28TrpfsTer12
NM_002878.3:c.81del , LRG_516t1:c.81del	NP_002869.3:p.Val28TrpfsTer12
NM_133629.2:c.81del	NP_598332.1:p.Val28TrpfsTer12
NR_037711.1:n.337del
NR_037712.1:n.337del
NR_037714.1:n.232+1758del
NM_001142571.2:c.81del	NP_001136043.1:p.Val28TrpfsTer12
NM_133629.3:c.81del	NP_598332.1:p.Val28TrpfsTer12
NR_037711.2:n.226del
NR_037712.2:n.226del
NM_002878.4:c.81del MANE Select	NP_002869.3:p.Val28TrpfsTer12