Canonical Allele Identifier: CA166969
Community Standard Title: NM_002878.4(RAD51D):c.629C>T (p.Ala210Val)
Gene: RAD51D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35103492G>A , CM000679.2:g.35103492G>A GRCh38
NC_000017.10:g.33430511G>A , CM000679.1:g.33430511G>A GRCh37
NC_000017.9:g.30454624G>A NCBI36
NG_031858.1:g.21378C>T , LRG_516:g.21378C>T

Transcript Alleles

HGVS Amino-acid Change
NM_002878.4:c.629C>T MANE Select NP_002869.3:p.Ala210Val
ENST00000345365.11:c.629C>T MANE Select ENSP00000338790.6:p.Ala210Val
NM_001142571.1:c.689C>T NP_001136043.1:p.Ala230Val
NM_001142571.2:c.689C>T NP_001136043.1:p.Ala230Val
NM_002878.3:c.629C>T , LRG_516t1:c.629C>T NP_002869.3:p.Ala210Val
NM_133629.2:c.293C>T NP_598332.1:p.Ala98Val
NM_133629.3:c.293C>T NP_598332.1:p.Ala98Val
NR_037711.1:n.766C>T
NR_037711.2:n.655C>T
NR_037712.1:n.631C>T
NR_037712.2:n.520C>T
NR_037714.1:n.381C>T
ENST00000335858.11:c.293C>T ENSP00000338408.6:p.Ala98Val
ENST00000345365.10:c.629C>T ENSP00000338790.6:p.Ala210Val
ENST00000394589.8:c.629C>T ENSP00000378090.4:p.Ala210Val
ENST00000460118.6:c.98C>T ENSP00000464356.2:p.Ala33Val
ENST00000586044.5:c.*360C>T ENSP00000465584.1:n.*360C>T
ENST00000586186.3:c.494C>T ENSP00000468273.3:p.Ala165Val
ENST00000586210.5:c.*223C>T ENSP00000465612.1:n.*223C>T
ENST00000587405.5:c.272C>T ENSP00000466478.1:p.Ala91Val
ENST00000587405.6:c.272C>T ENSP00000466478.2:p.Ala91Val
ENST00000587977.5:c.*369C>T ENSP00000466587.1:n.*369C>T
ENST00000588372.5:c.*112C>T ENSP00000468764.1:n.*112C>T
ENST00000588594.5:c.*225C>T ENSP00000465366.1:n.*225C>T
ENST00000590016.5:c.689C>T ENSP00000466399.1:p.Ala230Val
ENST00000590016.6:c.689C>T ENSP00000466399.1:p.Ala230Val
ENST00000591723.5:c.98C>T ENSP00000467986.1:p.Ala33Val
ENST00000592181.1:c.272C>T ENSP00000464799.1:p.Ala91Val
ENST00000592577.5:c.635C>T ENSP00000466839.1:p.Ala212Val
ENST00000592577.6:c.272C>T ENSP00000466839.2:p.Ala91Val
ENST00000593039.5:c.152C>T ENSP00000466834.1:p.Ala51Val