Canonical Allele Identifier: CA399086257

Gene: RAD51D

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35101206G>C , CM000679.2:g.35101206G>C	GRCh38
NC_000017.10:g.33428225G>C , CM000679.1:g.33428225G>C	GRCh37
NC_000017.9:g.30452338G>C	NCBI36
NG_031858.1:g.23664C>G , LRG_516:g.23664C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.763C>G	ENSP00000468273.3:p.Arg255Gly
ENST00000587405.6:c.541C>G	ENSP00000466478.2:p.Arg181Gly
ENST00000590016.6:c.958C>G	ENSP00000466399.1:p.Arg320Gly
ENST00000592577.6:c.541C>G	ENSP00000466839.2:p.Arg181Gly
ENST00000345365.11:c.898C>G MANE Select	ENSP00000338790.6:p.Arg300Gly
ENST00000335858.11:c.562C>G	ENSP00000338408.6:p.Arg188Gly
ENST00000345365.10:c.898C>G	ENSP00000338790.6:p.Arg300Gly
ENST00000394589.8:c.898C>G	ENSP00000378090.4:p.Arg300Gly
ENST00000460118.6:c.367C>G	ENSP00000464356.2:p.Arg123Gly
ENST00000586044.5:c.*629C>G	ENSP00000465584.1:n.*629C>G
ENST00000586210.5:c.*492C>G	ENSP00000465612.1:n.*492C>G
ENST00000587977.5:c.*638C>G	ENSP00000466587.1:n.*638C>G
ENST00000588372.5:c.*381C>G	ENSP00000468764.1:n.*381C>G
ENST00000588594.5:c.*494C>G	ENSP00000465366.1:n.*494C>G
ENST00000590016.5:c.958C>G	ENSP00000466399.1:p.Arg320Gly
ENST00000591723.5:c.367C>G	ENSP00000467986.1:p.Arg123Gly
ENST00000592181.1:c.541C>G	ENSP00000464799.1:p.Arg181Gly
ENST00000593039.5:c.421C>G	ENSP00000466834.1:p.Arg141Gly
NM_001142571.1:c.958C>G	NP_001136043.1:p.Arg320Gly
NM_002878.3:c.898C>G , LRG_516t1:c.898C>G	NP_002869.3:p.Arg300Gly
NM_133629.2:c.562C>G	NP_598332.1:p.Arg188Gly
NR_037711.1:n.1035C>G
NR_037712.1:n.900C>G
NR_037714.1:n.650C>G
NM_001142571.2:c.958C>G	NP_001136043.1:p.Arg320Gly
NM_133629.3:c.562C>G	NP_598332.1:p.Arg188Gly
NR_037711.2:n.924C>G
NR_037712.2:n.789C>G
NM_002878.4:c.898C>G MANE Select	NP_002869.3:p.Arg300Gly