Canonical Allele Identifier: CA2576232108
Gene: RAD51D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35119088G>T , CM000679.2:g.35119088G>T GRCh38
NC_000017.10:g.33446107G>T , CM000679.1:g.33446107G>T GRCh37
NC_000017.9:g.30470220G>T NCBI36
NG_031858.1:g.5782C>A , LRG_516:g.5782C>A
NG_054719.1:g.2510G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000586186.3:c.144+23C>A ENSP00000468273.3:n.144+23C>A
ENST00000587405.6:c.-95+2203C>A ENSP00000466478.2:n.-95+2203C>A
ENST00000590016.6:c.144+23C>A ENSP00000466399.1:n.144+23C>A
ENST00000590631.2:n.436+23C>A
ENST00000592577.6:c.-214+23C>A ENSP00000466839.2:n.-214+23C>A
ENST00000345365.11:c.144+23C>A MANE Select ENSP00000338790.6:n.144+23C>A
ENST00000335858.11:c.144+23C>A ENSP00000338408.6:n.144+23C>A
ENST00000345365.10:c.144+23C>A ENSP00000338790.6:n.144+23C>A
ENST00000394589.8:c.144+23C>A ENSP00000378090.4:n.144+23C>A
ENST00000415064.6:n.294+23C>A
ENST00000460118.6:c.-208+23C>A ENSP00000464356.2:n.-208+23C>A
ENST00000585343.5:c.47+23C>A
ENST00000585947.5:n.159+2203C>A
ENST00000585982.5:n.239+23C>A
ENST00000586044.5:c.144+23C>A ENSP00000465584.1:n.144+23C>A
ENST00000586186.2:c.47+23C>A
ENST00000586210.5:c.144+23C>A ENSP00000465612.1:n.144+23C>A
ENST00000587405.5:c.-95+2203C>A ENSP00000466478.1:n.-95+2203C>A
ENST00000587977.5:c.144+23C>A ENSP00000466587.1:n.144+23C>A
ENST00000587982.5:n.191+2203C>A
ENST00000588372.5:c.-95+2203C>A ENSP00000468764.1:n.-95+2203C>A
ENST00000588594.5:c.144+23C>A ENSP00000465366.1:n.144+23C>A
ENST00000589506.1:n.355+23C>A
ENST00000590016.5:c.144+23C>A ENSP00000466399.1:n.144+23C>A
ENST00000590631.1:c.-52+23C>A ENSP00000465033.1:n.-52+23C>A
ENST00000591723.5:c.-134+2203C>A ENSP00000467986.1:n.-134+2203C>A
ENST00000592181.1:c.-95+23C>A ENSP00000464799.1:n.-95+23C>A
ENST00000592430.5:n.232+2203C>A
ENST00000592577.5:c.150+23C>A ENSP00000466839.1:n.150+23C>A
ENST00000592850.5:c.47+23C>A
ENST00000592928.2:n.47+23C>A
ENST00000593039.5:c.3+2203C>A ENSP00000466834.1:n.3+2203C>A
NM_001142571.1:c.144+23C>A NP_001136043.1:n.144+23C>A
NM_002878.3:c.144+23C>A , LRG_516t1:c.144+23C>A NP_002869.3:n.144+23C>A
NM_133629.2:c.144+23C>A NP_598332.1:n.144+23C>A
NR_037711.1:n.400+23C>A
NR_037712.1:n.400+23C>A
NR_037714.1:n.232+2203C>A
NM_001142571.2:c.144+23C>A NP_001136043.1:n.144+23C>A
NM_133629.3:c.144+23C>A NP_598332.1:n.144+23C>A
NR_037711.2:n.289+23C>A
NR_037712.2:n.289+23C>A
NM_002878.4:c.144+23C>A MANE Select NP_002869.3:n.144+23C>A