Canonical Allele Identifier: CA3223488323
Community Standard Title: NM_002878.4(RAD51D):c.587C= (p.Ser196=)
Gene: RAD51D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35103534G= , CM000679.2:g.35103534G= GRCh38
NC_000017.10:g.33430553G= , CM000679.1:g.33430553G= GRCh37
NC_000017.9:g.30454666G= NCBI36
NG_031858.1:g.21336C= , LRG_516:g.21336C=

Transcript Alleles

HGVS Amino-acid Change
NM_002878.4:c.587C= MANE Select NP_002869.3:p.Ser196=
ENST00000345365.11:c.587C= MANE Select ENSP00000338790.6:p.Ser196=
NM_001142571.1:c.647C= NP_001136043.1:p.Ser216=
NM_001142571.2:c.647C= NP_001136043.1:p.Ser216=
NM_002878.3:c.587C= , LRG_516t1:c.587C= NP_002869.3:p.Ser196=
NM_133629.2:c.251C= NP_598332.1:p.Ser84=
NM_133629.3:c.251C= NP_598332.1:p.Ser84=
NR_037711.1:n.724C=
NR_037711.2:n.613C=
NR_037712.1:n.589C=
NR_037712.2:n.478C=
NR_037714.1:n.339C=
ENST00000335858.11:c.251C= ENSP00000338408.6:p.Ser84=
ENST00000345365.10:c.587C= ENSP00000338790.6:p.Ser196=
ENST00000394589.8:c.587C= ENSP00000378090.4:p.Ser196=
ENST00000460118.6:c.56C= ENSP00000464356.2:p.Ser19=
ENST00000586044.5:c.*318C= ENSP00000465584.1:n.*318C=
ENST00000586186.3:c.452C= ENSP00000468273.3:p.Ser151=
ENST00000586210.5:c.*181C= ENSP00000465612.1:n.*181C=
ENST00000587405.5:c.230C= ENSP00000466478.1:p.Ser77=
ENST00000587405.6:c.230C= ENSP00000466478.2:p.Ser77=
ENST00000587977.5:c.*327C= ENSP00000466587.1:n.*327C=
ENST00000588372.5:c.*70C= ENSP00000468764.1:n.*70C=
ENST00000588594.5:c.*183C= ENSP00000465366.1:n.*183C=
ENST00000590016.5:c.647C= ENSP00000466399.1:p.Ser216=
ENST00000590016.6:c.647C= ENSP00000466399.1:p.Ser216=
ENST00000590631.1:c.56C= ENSP00000465033.1:p.Ser19=
ENST00000590631.2:n.543C=
ENST00000591723.5:c.56C= ENSP00000467986.1:p.Ser19=
ENST00000592181.1:c.230C= ENSP00000464799.1:p.Ser77=
ENST00000592577.5:c.593C= ENSP00000466839.1:p.Ser198=
ENST00000592577.6:c.230C= ENSP00000466839.2:p.Ser77=
ENST00000593039.5:c.110C= ENSP00000466834.1:p.Ser37=