Canonical Allele Identifier: CA399086089

Gene: RAD51D

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35100985G>C , CM000679.2:g.35100985G>C	GRCh38
NC_000017.10:g.33428004G>C , CM000679.1:g.33428004G>C	GRCh37
NC_000017.9:g.30452117G>C	NCBI36
NG_031858.1:g.23885C>G , LRG_516:g.23885C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.820C>G	ENSP00000468273.3:p.Gln274Glu
ENST00000587405.6:c.598C>G	ENSP00000466478.2:p.Gln200Glu
ENST00000590016.6:c.1015C>G	ENSP00000466399.1:p.Gln339Glu
ENST00000592577.6:c.598C>G	ENSP00000466839.2:p.Gln200Glu
ENST00000345365.11:c.955C>G MANE Select	ENSP00000338790.6:p.Gln319Glu
ENST00000335858.11:c.619C>G	ENSP00000338408.6:p.Gln207Glu
ENST00000345365.10:c.955C>G	ENSP00000338790.6:p.Gln319Glu
ENST00000394589.8:c.955C>G	ENSP00000378090.4:p.Gln319Glu
ENST00000460118.6:c.424C>G	ENSP00000464356.2:p.Gln142Glu
ENST00000586044.5:c.*686C>G	ENSP00000465584.1:n.*686C>G
ENST00000586210.5:c.*549C>G	ENSP00000465612.1:n.*549C>G
ENST00000587977.5:c.*695C>G	ENSP00000466587.1:n.*695C>G
ENST00000588372.5:c.*438C>G	ENSP00000468764.1:n.*438C>G
ENST00000588594.5:c.*551C>G	ENSP00000465366.1:n.*551C>G
ENST00000590016.5:c.1015C>G	ENSP00000466399.1:p.Gln339Glu
ENST00000591723.5:c.372+216C>G	ENSP00000467986.1:n.372+216C>G
ENST00000592181.1:c.546+216C>G	ENSP00000464799.1:n.546+216C>G
ENST00000593039.5:c.426+216C>G	ENSP00000466834.1:n.426+216C>G
NM_001142571.1:c.1015C>G	NP_001136043.1:p.Gln339Glu
NM_002878.3:c.955C>G , LRG_516t1:c.955C>G	NP_002869.3:p.Gln319Glu
NM_133629.2:c.619C>G	NP_598332.1:p.Gln207Glu
NR_037711.1:n.1092C>G
NR_037712.1:n.957C>G
NR_037714.1:n.655+216C>G
NM_001142571.2:c.1015C>G	NP_001136043.1:p.Gln339Glu
NM_133629.3:c.619C>G	NP_598332.1:p.Gln207Glu
NR_037711.2:n.981C>G
NR_037712.2:n.846C>G
NM_002878.4:c.955C>G MANE Select	NP_002869.3:p.Gln319Glu