Canonical Allele Identifier: CA2257361847
Gene: RAD51D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35107027G= , CM000679.2:g.35107027G= GRCh38
NC_000017.10:g.33434046G= , CM000679.1:g.33434046G= GRCh37
NC_000017.9:g.30458159G= NCBI36
NG_031858.1:g.17843C= , LRG_516:g.17843C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000586186.3:c.345+339C= ENSP00000468273.3:n.345+339C=
ENST00000587405.6:c.84C= ENSP00000466478.2:p.Leu28=
ENST00000590016.6:c.501C= ENSP00000466399.1:p.Leu167=
ENST00000590631.2:n.437-546C=
ENST00000592577.6:c.84C= ENSP00000466839.2:p.Leu28=
ENST00000345365.11:c.441C= MANE Select ENSP00000338790.6:p.Leu147=
ENST00000335858.11:c.145-546C= ENSP00000338408.6:n.145-546C=
ENST00000345365.10:c.441C= ENSP00000338790.6:p.Leu147=
ENST00000394589.8:c.441C= ENSP00000378090.4:p.Leu147=
ENST00000415064.6:n.591C=
ENST00000460118.6:c.-91C= ENSP00000464356.2:n.-91C=
ENST00000585343.5:c.523C=
ENST00000585947.5:n.337C=
ENST00000585982.5:n.500+339C=
ENST00000586044.5:c.*172C= ENSP00000465584.1:n.*172C=
ENST00000586186.2:c.248+339C=
ENST00000586210.5:c.*35C= ENSP00000465612.1:n.*35C=
ENST00000587405.5:c.84C= ENSP00000466478.1:p.Leu28=
ENST00000587977.5:c.*181C= ENSP00000466587.1:n.*181C=
ENST00000587982.5:n.273+339C=
ENST00000588372.5:c.84C= ENSP00000468764.1:p.Leu28=
ENST00000588594.5:c.*76+339C= ENSP00000465366.1:n.*76+339C=
ENST00000590016.5:c.501C= ENSP00000466399.1:p.Leu167=
ENST00000590631.1:c.-51-546C= ENSP00000465033.1:n.-51-546C=
ENST00000591723.5:c.-52+339C= ENSP00000467986.1:n.-52+339C=
ENST00000592181.1:c.84C= ENSP00000464799.1:p.Leu28=
ENST00000592430.5:n.410C=
ENST00000592577.5:c.447C= ENSP00000466839.1:p.Leu149=
ENST00000592850.5:c.346-546C=
ENST00000592928.2:n.167-546C=
ENST00000593039.5:c.4-546C= ENSP00000466834.1:n.4-546C=
NM_001142571.1:c.501C= NP_001136043.1:p.Leu167=
NM_002878.3:c.441C= , LRG_516t1:c.441C= NP_002869.3:p.Leu147=
NM_133629.2:c.145-546C= NP_598332.1:n.145-546C=
NR_037711.1:n.578C=
NR_037712.1:n.482+339C=
NR_037714.1:n.233-546C=
NM_001142571.2:c.501C= NP_001136043.1:p.Leu167=
NM_133629.3:c.145-546C= NP_598332.1:n.145-546C=
NR_037711.2:n.467C=
NR_037712.2:n.371+339C=
NM_002878.4:c.441C= MANE Select NP_002869.3:p.Leu147=