Canonical Allele Identifier: CA399088504

Gene: RAD51D

Linked Data

• dbSNP Id: rs876660090
• MyVariant Identifiers: chr17:g.33433406T>A (hg19) ; chr17:g.35106387T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35106387T>A , CM000679.2:g.35106387T>A	GRCh38
NC_000017.10:g.33433406T>A , CM000679.1:g.33433406T>A	GRCh37
NC_000017.9:g.30457519T>A	NCBI36
NG_031858.1:g.18483A>T , LRG_516:g.18483A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000586186.3:c.440A>T	ENSP00000468273.3:p.Gln147Leu
ENST00000587405.6:c.218A>T	ENSP00000466478.2:p.Gln73Leu
ENST00000590016.6:c.635A>T	ENSP00000466399.1:p.Gln212Leu
ENST00000590631.2:n.531A>T
ENST00000592577.6:c.218A>T	ENSP00000466839.2:p.Gln73Leu
ENST00000345365.11:c.575A>T MANE Select	ENSP00000338790.6:p.Gln192Leu
ENST00000335858.11:c.239A>T	ENSP00000338408.6:p.Gln80Leu
ENST00000345365.10:c.575A>T	ENSP00000338790.6:p.Gln192Leu
ENST00000394589.8:c.575A>T	ENSP00000378090.4:p.Gln192Leu
ENST00000415064.6:n.725A>T
ENST00000460118.6:c.44A>T	ENSP00000464356.2:p.Gln15Leu
ENST00000585947.5:n.471A>T
ENST00000585982.5:n.595A>T
ENST00000586044.5:c.*306A>T	ENSP00000465584.1:n.*306A>T
ENST00000586210.5:c.*169A>T	ENSP00000465612.1:n.*169A>T
ENST00000587405.5:c.218A>T	ENSP00000466478.1:p.Gln73Leu
ENST00000587977.5:c.*315A>T	ENSP00000466587.1:n.*315A>T
ENST00000587982.5:n.368A>T
ENST00000588372.5:c.218A>T	ENSP00000468764.1:p.Gln73Leu
ENST00000588594.5:c.*171A>T	ENSP00000465366.1:n.*171A>T
ENST00000590016.5:c.635A>T	ENSP00000466399.1:p.Gln212Leu
ENST00000590631.1:c.44A>T	ENSP00000465033.1:p.Gln15Leu
ENST00000591723.5:c.44A>T	ENSP00000467986.1:p.Gln15Leu
ENST00000592181.1:c.218A>T	ENSP00000464799.1:p.Gln73Leu
ENST00000592430.5:n.544A>T
ENST00000592577.5:c.581A>T	ENSP00000466839.1:p.Gln194Leu
ENST00000593039.5:c.98A>T	ENSP00000466834.1:p.Gln33Leu
NM_001142571.1:c.635A>T	NP_001136043.1:p.Gln212Leu
NM_002878.3:c.575A>T , LRG_516t1:c.575A>T	NP_002869.3:p.Gln192Leu
NM_133629.2:c.239A>T	NP_598332.1:p.Gln80Leu
NR_037711.1:n.712A>T
NR_037712.1:n.577A>T
NR_037714.1:n.327A>T
NM_001142571.2:c.635A>T	NP_001136043.1:p.Gln212Leu
NM_133629.3:c.239A>T	NP_598332.1:p.Gln80Leu
NR_037711.2:n.601A>T
NR_037712.2:n.466A>T
NM_002878.4:c.575A>T MANE Select	NP_002869.3:p.Gln192Leu