Canonical Allele Identifier: CA399088492

Gene: RAD51D

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35106385C>A , CM000679.2:g.35106385C>A	GRCh38
NC_000017.10:g.33433404C>A , CM000679.1:g.33433404C>A	GRCh37
NC_000017.9:g.30457517C>A	NCBI36
NG_031858.1:g.18485G>T , LRG_516:g.18485G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.441+1G>T	ENSP00000468273.3:n.441+1G>T
ENST00000587405.6:c.219+1G>T	ENSP00000466478.2:n.219+1G>T
ENST00000590016.6:c.636+1G>T	ENSP00000466399.1:n.636+1G>T
ENST00000590631.2:n.532+1G>T
ENST00000592577.6:c.219+1G>T	ENSP00000466839.2:n.219+1G>T
ENST00000345365.11:c.576+1G>T MANE Select	ENSP00000338790.6:n.576+1G>T
ENST00000335858.11:c.240+1G>T	ENSP00000338408.6:n.240+1G>T
ENST00000345365.10:c.576+1G>T	ENSP00000338790.6:n.576+1G>T
ENST00000394589.8:c.576+1G>T	ENSP00000378090.4:n.576+1G>T
ENST00000415064.6:n.726+1G>T
ENST00000460118.6:c.45+1G>T	ENSP00000464356.2:n.45+1G>T
ENST00000585947.5:n.473G>T
ENST00000586044.5:c.*307+1G>T	ENSP00000465584.1:n.*307+1G>T
ENST00000586210.5:c.*170+1G>T	ENSP00000465612.1:n.*170+1G>T
ENST00000587405.5:c.219+1G>T	ENSP00000466478.1:n.219+1G>T
ENST00000587977.5:c.*316+1G>T	ENSP00000466587.1:n.*316+1G>T
ENST00000587982.5:n.370G>T
ENST00000588372.5:c.219+1G>T	ENSP00000468764.1:n.219+1G>T
ENST00000588594.5:c.*172+1G>T	ENSP00000465366.1:n.*172+1G>T
ENST00000590016.5:c.636+1G>T	ENSP00000466399.1:n.636+1G>T
ENST00000590631.1:c.45+1G>T	ENSP00000465033.1:n.45+1G>T
ENST00000591723.5:c.45+1G>T	ENSP00000467986.1:n.45+1G>T
ENST00000592181.1:c.219+1G>T	ENSP00000464799.1:n.219+1G>T
ENST00000592430.5:n.545+1G>T
ENST00000592577.5:c.582+1G>T	ENSP00000466839.1:n.582+1G>T
ENST00000593039.5:c.99+1G>T	ENSP00000466834.1:n.99+1G>T
NM_001142571.1:c.636+1G>T	NP_001136043.1:n.636+1G>T
NM_002878.3:c.576+1G>T , LRG_516t1:c.576+1G>T	NP_002869.3:n.576+1G>T
NM_133629.2:c.240+1G>T	NP_598332.1:n.240+1G>T
NR_037711.1:n.713+1G>T
NR_037712.1:n.578+1G>T
NR_037714.1:n.328+1G>T
NM_001142571.2:c.636+1G>T	NP_001136043.1:n.636+1G>T
NM_133629.3:c.240+1G>T	NP_598332.1:n.240+1G>T
NR_037711.2:n.602+1G>T
NR_037712.2:n.467+1G>T
NM_002878.4:c.576+1G>T MANE Select	NP_002869.3:n.576+1G>T