Canonical Allele Identifier: CA165041
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 141300
dbSNP Id: rs540273429

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35101353T>C , CM000679.2:g.35101353T>C GRCh38
NC_000017.10:g.33428372T>C , CM000679.1:g.33428372T>C GRCh37
NC_000017.9:g.30452485T>C NCBI36
NG_031858.1:g.23517A>G , LRG_516:g.23517A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000586186.3:c.616A>G ENSP00000468273.3:p.Ile206Val
ENST00000587405.6:c.394A>G ENSP00000466478.2:p.Ile132Val
ENST00000590016.6:c.811A>G ENSP00000466399.1:p.Ile271Val
ENST00000592577.6:c.394A>G ENSP00000466839.2:p.Ile132Val
ENST00000345365.11:c.751A>G MANE Select ENSP00000338790.6:p.Ile251Val
ENST00000335858.11:c.415A>G ENSP00000338408.6:p.Ile139Val
ENST00000345365.10:c.751A>G ENSP00000338790.6:p.Ile251Val
ENST00000394589.8:c.751A>G ENSP00000378090.4:p.Ile251Val
ENST00000460118.6:c.220A>G ENSP00000464356.2:p.Ile74Val
ENST00000586044.5:c.*482A>G ENSP00000465584.1:n.*482A>G
ENST00000586210.5:c.*345A>G ENSP00000465612.1:n.*345A>G
ENST00000587405.5:c.394A>G ENSP00000466478.1:p.Ile132Val
ENST00000587977.5:c.*491A>G ENSP00000466587.1:n.*491A>G
ENST00000588372.5:c.*234A>G ENSP00000468764.1:n.*234A>G
ENST00000588594.5:c.*347A>G ENSP00000465366.1:n.*347A>G
ENST00000590016.5:c.811A>G ENSP00000466399.1:p.Ile271Val
ENST00000591723.5:c.220A>G ENSP00000467986.1:p.Ile74Val
ENST00000592181.1:c.394A>G ENSP00000464799.1:p.Ile132Val
ENST00000593039.5:c.274A>G ENSP00000466834.1:p.Ile92Val
NM_001142571.1:c.811A>G NP_001136043.1:p.Ile271Val
NM_002878.3:c.751A>G , LRG_516t1:c.751A>G NP_002869.3:p.Ile251Val
NM_133629.2:c.415A>G NP_598332.1:p.Ile139Val
NR_037711.1:n.888A>G
NR_037712.1:n.753A>G
NR_037714.1:n.503A>G
NM_001142571.2:c.811A>G NP_001136043.1:p.Ile271Val
NM_133629.3:c.415A>G NP_598332.1:p.Ile139Val
NR_037711.2:n.777A>G
NR_037712.2:n.642A>G
NM_002878.4:c.751A>G MANE Select NP_002869.3:p.Ile251Val