Canonical Allele Identifier: CA399086806

Gene: RAD51D

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35101301C>G , CM000679.2:g.35101301C>G	GRCh38
NC_000017.10:g.33428320C>G , CM000679.1:g.33428320C>G	GRCh37
NC_000017.9:g.30452433C>G	NCBI36
NG_031858.1:g.23569G>C , LRG_516:g.23569G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.668G>C	ENSP00000468273.3:p.Trp223Ser
ENST00000587405.6:c.446G>C	ENSP00000466478.2:p.Trp149Ser
ENST00000590016.6:c.863G>C	ENSP00000466399.1:p.Trp288Ser
ENST00000592577.6:c.446G>C	ENSP00000466839.2:p.Trp149Ser
ENST00000345365.11:c.803G>C MANE Select	ENSP00000338790.6:p.Trp268Ser
ENST00000335858.11:c.467G>C	ENSP00000338408.6:p.Trp156Ser
ENST00000345365.10:c.803G>C	ENSP00000338790.6:p.Trp268Ser
ENST00000394589.8:c.803G>C	ENSP00000378090.4:p.Trp268Ser
ENST00000460118.6:c.272G>C	ENSP00000464356.2:p.Trp91Ser
ENST00000586044.5:c.*534G>C	ENSP00000465584.1:n.*534G>C
ENST00000586210.5:c.*397G>C	ENSP00000465612.1:n.*397G>C
ENST00000587977.5:c.*543G>C	ENSP00000466587.1:n.*543G>C
ENST00000588372.5:c.*286G>C	ENSP00000468764.1:n.*286G>C
ENST00000588594.5:c.*399G>C	ENSP00000465366.1:n.*399G>C
ENST00000590016.5:c.863G>C	ENSP00000466399.1:p.Trp288Ser
ENST00000591723.5:c.272G>C	ENSP00000467986.1:p.Trp91Ser
ENST00000592181.1:c.446G>C	ENSP00000464799.1:p.Trp149Ser
ENST00000593039.5:c.326G>C	ENSP00000466834.1:p.Trp109Ser
NM_001142571.1:c.863G>C	NP_001136043.1:p.Trp288Ser
NM_002878.3:c.803G>C , LRG_516t1:c.803G>C	NP_002869.3:p.Trp268Ser
NM_133629.2:c.467G>C	NP_598332.1:p.Trp156Ser
NR_037711.1:n.940G>C
NR_037712.1:n.805G>C
NR_037714.1:n.555G>C
NM_001142571.2:c.863G>C	NP_001136043.1:p.Trp288Ser
NM_133629.3:c.467G>C	NP_598332.1:p.Trp156Ser
NR_037711.2:n.829G>C
NR_037712.2:n.694G>C
NM_002878.4:c.803G>C MANE Select	NP_002869.3:p.Trp268Ser