Canonical Allele Identifier: CA198479
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 187753
dbSNP Id: rs786203974

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35100961G>A , CM000679.2:g.35100961G>A GRCh38
NC_000017.10:g.33427980G>A , CM000679.1:g.33427980G>A GRCh37
NC_000017.9:g.30452093G>A NCBI36
NG_031858.1:g.23909C>T , LRG_516:g.23909C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000586186.3:c.844C>T ENSP00000468273.3:p.Gln282Ter
ENST00000587405.6:c.622C>T ENSP00000466478.2:p.Gln208Ter
ENST00000590016.6:c.1039C>T ENSP00000466399.1:p.Gln347Ter
ENST00000592577.6:c.622C>T ENSP00000466839.2:p.Gln208Ter
ENST00000345365.11:c.979C>T MANE Select ENSP00000338790.6:p.Gln327Ter
ENST00000335858.11:c.643C>T ENSP00000338408.6:p.Gln215Ter
ENST00000345365.10:c.979C>T ENSP00000338790.6:p.Gln327Ter
ENST00000394589.8:c.979C>T ENSP00000378090.4:p.Gln327Ter
ENST00000460118.6:c.448C>T ENSP00000464356.2:p.Gln150Ter
ENST00000586044.5:c.*710C>T ENSP00000465584.1:n.*710C>T
ENST00000586210.5:c.*573C>T ENSP00000465612.1:n.*573C>T
ENST00000587977.5:c.*719C>T ENSP00000466587.1:n.*719C>T
ENST00000588372.5:c.*462C>T ENSP00000468764.1:n.*462C>T
ENST00000588594.5:c.*575C>T ENSP00000465366.1:n.*575C>T
ENST00000590016.5:c.1039C>T ENSP00000466399.1:p.Gln347Ter
ENST00000591723.5:c.372+240C>T ENSP00000467986.1:n.372+240C>T
ENST00000592181.1:c.546+240C>T ENSP00000464799.1:n.546+240C>T
ENST00000593039.5:c.426+240C>T ENSP00000466834.1:n.426+240C>T
NM_001142571.1:c.1039C>T NP_001136043.1:p.Gln347Ter
NM_002878.3:c.979C>T , LRG_516t1:c.979C>T NP_002869.3:p.Gln327Ter
NM_133629.2:c.643C>T NP_598332.1:p.Gln215Ter
NR_037711.1:n.1116C>T
NR_037712.1:n.981C>T
NR_037714.1:n.655+240C>T
NM_001142571.2:c.1039C>T NP_001136043.1:p.Gln347Ter
NM_133629.3:c.643C>T NP_598332.1:p.Gln215Ter
NR_037711.2:n.1005C>T
NR_037712.2:n.870C>T
NM_002878.4:c.979C>T MANE Select NP_002869.3:p.Gln327Ter