Canonical Allele Identifier: CA2257334950
Gene: RAD51D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35107109A= , CM000679.2:g.35107109A= GRCh38
NC_000017.10:g.33434128A= , CM000679.1:g.33434128A= GRCh37
NC_000017.9:g.30458241A= NCBI36
NG_031858.1:g.17761T= , LRG_516:g.17761T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000586186.3:c.345+257T= ENSP00000468273.3:n.345+257T=
ENST00000587405.6:c.2T= ENSP00000466478.2:p.Met1=
ENST00000590016.6:c.419T= ENSP00000466399.1:p.Met140=
ENST00000590631.2:n.437-628T=
ENST00000592577.6:c.2T= ENSP00000466839.2:p.Met1=
ENST00000345365.11:c.359T= MANE Select ENSP00000338790.6:p.Met120=
ENST00000335858.11:c.145-628T= ENSP00000338408.6:n.145-628T=
ENST00000345365.10:c.359T= ENSP00000338790.6:p.Met120=
ENST00000394589.8:c.359T= ENSP00000378090.4:p.Met120=
ENST00000415064.6:n.509T=
ENST00000460118.6:c.-125-48T= ENSP00000464356.2:n.-125-48T=
ENST00000585343.5:c.441T=
ENST00000585947.5:n.255T=
ENST00000585982.5:n.500+257T=
ENST00000586044.5:c.*90T= ENSP00000465584.1:n.*90T=
ENST00000586186.2:c.248+257T=
ENST00000586210.5:c.277T= ENSP00000465612.1:p.Trp93=
ENST00000587405.5:c.2T= ENSP00000466478.1:p.Met1=
ENST00000587977.5:c.*99T= ENSP00000466587.1:n.*99T=
ENST00000587982.5:n.273+257T=
ENST00000588372.5:c.2T= ENSP00000468764.1:p.Met1=
ENST00000588594.5:c.*76+257T= ENSP00000465366.1:n.*76+257T=
ENST00000590016.5:c.419T= ENSP00000466399.1:p.Met140=
ENST00000590631.1:c.-51-628T= ENSP00000465033.1:n.-51-628T=
ENST00000591723.5:c.-52+257T= ENSP00000467986.1:n.-52+257T=
ENST00000592181.1:c.2T= ENSP00000464799.1:p.Met1=
ENST00000592430.5:n.328T=
ENST00000592577.5:c.365T= ENSP00000466839.1:p.Met122=
ENST00000592850.5:c.346-628T=
ENST00000592928.2:n.167-628T=
ENST00000593039.5:c.4-628T= ENSP00000466834.1:n.4-628T=
NM_001142571.1:c.419T= NP_001136043.1:p.Met140=
NM_002878.3:c.359T= , LRG_516t1:c.359T= NP_002869.3:p.Met120=
NM_133629.2:c.145-628T= NP_598332.1:n.145-628T=
NR_037711.1:n.496T=
NR_037712.1:n.482+257T=
NR_037714.1:n.233-628T=
NM_001142571.2:c.419T= NP_001136043.1:p.Met140=
NM_133629.3:c.145-628T= NP_598332.1:n.145-628T=
NR_037711.2:n.385T=
NR_037712.2:n.371+257T=
NM_002878.4:c.359T= MANE Select NP_002869.3:p.Met120=