Canonical Allele Identifier: CA399086064

Gene: RAD51D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35100973A>C , CM000679.2:g.35100973A>C	GRCh38
NC_000017.10:g.33427992A>C , CM000679.1:g.33427992A>C	GRCh37
NC_000017.9:g.30452105A>C	NCBI36
NG_031858.1:g.23897T>G , LRG_516:g.23897T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.832T>G	ENSP00000468273.3:p.Leu278Val
ENST00000587405.6:c.610T>G	ENSP00000466478.2:p.Leu204Val
ENST00000590016.6:c.1027T>G	ENSP00000466399.1:p.Leu343Val
ENST00000592577.6:c.610T>G	ENSP00000466839.2:p.Leu204Val
ENST00000345365.11:c.967T>G MANE Select	ENSP00000338790.6:p.Leu323Val
ENST00000335858.11:c.631T>G	ENSP00000338408.6:p.Leu211Val
ENST00000345365.10:c.967T>G	ENSP00000338790.6:p.Leu323Val
ENST00000394589.8:c.967T>G	ENSP00000378090.4:p.Leu323Val
ENST00000460118.6:c.436T>G	ENSP00000464356.2:p.Leu146Val
ENST00000586044.5:c.*698T>G	ENSP00000465584.1:n.*698T>G
ENST00000586210.5:c.*561T>G	ENSP00000465612.1:n.*561T>G
ENST00000587977.5:c.*707T>G	ENSP00000466587.1:n.*707T>G
ENST00000588372.5:c.*450T>G	ENSP00000468764.1:n.*450T>G
ENST00000588594.5:c.*563T>G	ENSP00000465366.1:n.*563T>G
ENST00000590016.5:c.1027T>G	ENSP00000466399.1:p.Leu343Val
ENST00000591723.5:c.372+228T>G	ENSP00000467986.1:n.372+228T>G
ENST00000592181.1:c.546+228T>G	ENSP00000464799.1:n.546+228T>G
ENST00000593039.5:c.426+228T>G	ENSP00000466834.1:n.426+228T>G
NM_001142571.1:c.1027T>G	NP_001136043.1:p.Leu343Val
NM_002878.3:c.967T>G , LRG_516t1:c.967T>G	NP_002869.3:p.Leu323Val
NM_133629.2:c.631T>G	NP_598332.1:p.Leu211Val
NR_037711.1:n.1104T>G
NR_037712.1:n.969T>G
NR_037714.1:n.655+228T>G
NM_001142571.2:c.1027T>G	NP_001136043.1:p.Leu343Val
NM_133629.3:c.631T>G	NP_598332.1:p.Leu211Val
NR_037711.2:n.993T>G
NR_037712.2:n.858T>G
NM_002878.4:c.967T>G MANE Select	NP_002869.3:p.Leu323Val