Canonical Allele Identifier: CA399091169

Gene: RAD51D

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35118499A>T , CM000679.2:g.35118499A>T	GRCh38
NC_000017.10:g.33445518A>T , CM000679.1:g.33445518A>T	GRCh37
NC_000017.9:g.30469631A>T	NCBI36
NG_031858.1:g.6371T>A , LRG_516:g.6371T>A
NG_054719.1:g.1921A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.263+2T>A	ENSP00000468273.3:n.263+2T>A
ENST00000587405.6:c.-95+2792T>A	ENSP00000466478.2:n.-95+2792T>A
ENST00000590016.6:c.144+612T>A	ENSP00000466399.1:n.144+612T>A
ENST00000590631.2:n.436+612T>A
ENST00000592577.6:c.-95+2T>A	ENSP00000466839.2:n.-95+2T>A
ENST00000345365.11:c.263+2T>A MANE Select	ENSP00000338790.6:n.263+2T>A
ENST00000335858.11:c.144+612T>A	ENSP00000338408.6:n.144+612T>A
ENST00000345365.10:c.263+2T>A	ENSP00000338790.6:n.263+2T>A
ENST00000394589.8:c.263+2T>A	ENSP00000378090.4:n.263+2T>A
ENST00000415064.6:n.413+2T>A
ENST00000460118.6:c.-208+612T>A	ENSP00000464356.2:n.-208+612T>A
ENST00000585343.5:c.166+2T>A
ENST00000585947.5:n.159+2792T>A
ENST00000585982.5:n.239+612T>A
ENST00000586044.5:c.144+612T>A	ENSP00000465584.1:n.144+612T>A
ENST00000586186.2:c.166+2T>A
ENST00000586210.5:c.263+2T>A	ENSP00000465612.1:n.263+2T>A
ENST00000587405.5:c.-95+2792T>A	ENSP00000466478.1:n.-95+2792T>A
ENST00000587977.5:c.263+2T>A	ENSP00000466587.1:n.263+2T>A
ENST00000587982.5:n.191+2792T>A
ENST00000588372.5:c.-95+2792T>A	ENSP00000468764.1:n.-95+2792T>A
ENST00000588594.5:c.144+612T>A	ENSP00000465366.1:n.144+612T>A
ENST00000589506.1:n.355+612T>A
ENST00000590016.5:c.144+612T>A	ENSP00000466399.1:n.144+612T>A
ENST00000590631.1:c.-52+612T>A	ENSP00000465033.1:n.-52+612T>A
ENST00000591723.5:c.-134+2792T>A	ENSP00000467986.1:n.-134+2792T>A
ENST00000592181.1:c.-95+612T>A	ENSP00000464799.1:n.-95+612T>A
ENST00000592430.5:n.232+2792T>A
ENST00000592577.5:c.269+2T>A	ENSP00000466839.1:n.269+2T>A
ENST00000592850.5:c.166+2T>A
ENST00000592928.2:n.166+2T>A
ENST00000593039.5:c.3+2792T>A	ENSP00000466834.1:n.3+2792T>A
NM_001142571.1:c.144+612T>A	NP_001136043.1:n.144+612T>A
NM_002878.3:c.263+2T>A , LRG_516t1:c.263+2T>A	NP_002869.3:n.263+2T>A
NM_133629.2:c.144+612T>A	NP_598332.1:n.144+612T>A
NR_037711.1:n.400+612T>A
NR_037712.1:n.400+612T>A
NR_037714.1:n.232+2792T>A
NM_001142571.2:c.144+612T>A	NP_001136043.1:n.144+612T>A
NM_133629.3:c.144+612T>A	NP_598332.1:n.144+612T>A
NR_037711.2:n.289+612T>A
NR_037712.2:n.289+612T>A
NM_002878.4:c.263+2T>A MANE Select	NP_002869.3:n.263+2T>A