Canonical Allele Identifier: CA399089403

Gene: RAD51D

Linked Data

• dbSNP Id: rs2142434017
• MyVariant Identifiers: chr17:g.33434137C>T (hg19) ; chr17:g.35107118C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35107118C>T , CM000679.2:g.35107118C>T	GRCh38
NC_000017.10:g.33434137C>T , CM000679.1:g.33434137C>T	GRCh37
NC_000017.9:g.30458250C>T	NCBI36
NG_031858.1:g.17752G>A , LRG_516:g.17752G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.345+248G>A	ENSP00000468273.3:n.345+248G>A
ENST00000587405.6:c.-8G>A	ENSP00000466478.2:n.-8G>A
ENST00000590016.6:c.410G>A	ENSP00000466399.1:p.Cys137Tyr
ENST00000590631.2:n.437-637G>A
ENST00000592577.6:c.-8G>A	ENSP00000466839.2:n.-8G>A
ENST00000345365.11:c.350G>A MANE Select	ENSP00000338790.6:p.Cys117Tyr
ENST00000335858.11:c.145-637G>A	ENSP00000338408.6:n.145-637G>A
ENST00000345365.10:c.350G>A	ENSP00000338790.6:p.Cys117Tyr
ENST00000394589.8:c.350G>A	ENSP00000378090.4:p.Cys117Tyr
ENST00000415064.6:n.500G>A
ENST00000460118.6:c.-125-57G>A	ENSP00000464356.2:n.-125-57G>A
ENST00000585343.5:c.432G>A
ENST00000585947.5:n.246G>A
ENST00000585982.5:n.500+248G>A
ENST00000586044.5:c.*81G>A	ENSP00000465584.1:n.*81G>A
ENST00000586186.2:c.248+248G>A
ENST00000586210.5:c.268G>A	ENSP00000465612.1:p.Val90Ile
ENST00000587405.5:c.-8G>A	ENSP00000466478.1:n.-8G>A
ENST00000587977.5:c.*90G>A	ENSP00000466587.1:n.*90G>A
ENST00000587982.5:n.273+248G>A
ENST00000588372.5:c.-8G>A	ENSP00000468764.1:n.-8G>A
ENST00000588594.5:c.*76+248G>A	ENSP00000465366.1:n.*76+248G>A
ENST00000590016.5:c.410G>A	ENSP00000466399.1:p.Cys137Tyr
ENST00000590631.1:c.-51-637G>A	ENSP00000465033.1:n.-51-637G>A
ENST00000591723.5:c.-52+248G>A	ENSP00000467986.1:n.-52+248G>A
ENST00000592181.1:c.-8G>A	ENSP00000464799.1:n.-8G>A
ENST00000592430.5:n.319G>A
ENST00000592577.5:c.356G>A	ENSP00000466839.1:p.Cys119Tyr
ENST00000592850.5:c.346-637G>A
ENST00000592928.2:n.167-637G>A
ENST00000593039.5:c.4-637G>A	ENSP00000466834.1:n.4-637G>A
NM_001142571.1:c.410G>A	NP_001136043.1:p.Cys137Tyr
NM_002878.3:c.350G>A , LRG_516t1:c.350G>A	NP_002869.3:p.Cys117Tyr
NM_133629.2:c.145-637G>A	NP_598332.1:n.145-637G>A
NR_037711.1:n.487G>A
NR_037712.1:n.482+248G>A
NR_037714.1:n.233-637G>A
NM_001142571.2:c.410G>A	NP_001136043.1:p.Cys137Tyr
NM_133629.3:c.145-637G>A	NP_598332.1:n.145-637G>A
NR_037711.2:n.376G>A
NR_037712.2:n.371+248G>A
NM_002878.4:c.350G>A MANE Select	NP_002869.3:p.Cys117Tyr