Canonical Allele Identifier: CA299922

Gene: RAD51D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35101047A>T , CM000679.2:g.35101047A>T	GRCh38
NC_000017.10:g.33428066A>T , CM000679.1:g.33428066A>T	GRCh37
NC_000017.9:g.30452179A>T	NCBI36
NG_031858.1:g.23823T>A , LRG_516:g.23823T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002878.4:c.904-11T>A MANE Select	NP_002869.3:n.904-11T>A
ENST00000345365.11:c.904-11T>A MANE Select	ENSP00000338790.6:n.904-11T>A
NM_001142571.1:c.964-11T>A	NP_001136043.1:n.964-11T>A
NM_001142571.2:c.964-11T>A	NP_001136043.1:n.964-11T>A
NM_002878.3:c.904-11T>A , LRG_516t1:c.904-11T>A	NP_002869.3:n.904-11T>A
NM_133629.2:c.568-11T>A	NP_598332.1:n.568-11T>A
NM_133629.3:c.568-11T>A	NP_598332.1:n.568-11T>A
NR_037711.1:n.1041-11T>A
NR_037711.2:n.930-11T>A
NR_037712.1:n.906-11T>A
NR_037712.2:n.795-11T>A
NR_037714.1:n.655+154T>A
ENST00000335858.11:c.568-11T>A	ENSP00000338408.6:n.568-11T>A
ENST00000345365.10:c.904-11T>A	ENSP00000338790.6:n.904-11T>A
ENST00000394589.8:c.904-11T>A	ENSP00000378090.4:n.904-11T>A
ENST00000460118.6:c.373-11T>A	ENSP00000464356.2:n.373-11T>A
ENST00000586044.5:c.*635-11T>A	ENSP00000465584.1:n.*635-11T>A
ENST00000586186.3:c.769-11T>A	ENSP00000468273.3:n.769-11T>A
ENST00000586210.5:c.*498-11T>A	ENSP00000465612.1:n.*498-11T>A
ENST00000587405.6:c.547-11T>A	ENSP00000466478.2:n.547-11T>A
ENST00000587977.5:c.*644-11T>A	ENSP00000466587.1:n.*644-11T>A
ENST00000588372.5:c.*387-11T>A	ENSP00000468764.1:n.*387-11T>A
ENST00000588594.5:c.*500-11T>A	ENSP00000465366.1:n.*500-11T>A
ENST00000590016.5:c.964-11T>A	ENSP00000466399.1:n.964-11T>A
ENST00000590016.6:c.964-11T>A	ENSP00000466399.1:n.964-11T>A
ENST00000591723.5:c.372+154T>A	ENSP00000467986.1:n.372+154T>A
ENST00000592181.1:c.546+154T>A	ENSP00000464799.1:n.546+154T>A
ENST00000592577.6:c.547-11T>A	ENSP00000466839.2:n.547-11T>A
ENST00000593039.5:c.426+154T>A	ENSP00000466834.1:n.426+154T>A