Canonical Allele Identifier: CA399089287

Gene: RAD51D

Linked Data

• dbSNP Id: rs2142433158
• MyVariant Identifiers: chr17:g.33434081C>T (hg19) ; chr17:g.35107062C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35107062C>T , CM000679.2:g.35107062C>T	GRCh38
NC_000017.10:g.33434081C>T , CM000679.1:g.33434081C>T	GRCh37
NC_000017.9:g.30458194C>T	NCBI36
NG_031858.1:g.17808G>A , LRG_516:g.17808G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.345+304G>A	ENSP00000468273.3:n.345+304G>A
ENST00000587405.6:c.49G>A	ENSP00000466478.2:p.Asp17Asn
ENST00000590016.6:c.466G>A	ENSP00000466399.1:p.Asp156Asn
ENST00000590631.2:n.437-581G>A
ENST00000592577.6:c.49G>A	ENSP00000466839.2:p.Asp17Asn
ENST00000345365.11:c.406G>A MANE Select	ENSP00000338790.6:p.Asp136Asn
ENST00000335858.11:c.145-581G>A	ENSP00000338408.6:n.145-581G>A
ENST00000345365.10:c.406G>A	ENSP00000338790.6:p.Asp136Asn
ENST00000394589.8:c.406G>A	ENSP00000378090.4:p.Asp136Asn
ENST00000415064.6:n.556G>A
ENST00000460118.6:c.-125-1G>A	ENSP00000464356.2:n.-125-1G>A
ENST00000585343.5:c.488G>A
ENST00000585947.5:n.302G>A
ENST00000585982.5:n.500+304G>A
ENST00000586044.5:c.*137G>A	ENSP00000465584.1:n.*137G>A
ENST00000586186.2:c.248+304G>A
ENST00000586210.5:c.324G>A	ENSP00000465612.1:p.Ter108=
ENST00000587405.5:c.49G>A	ENSP00000466478.1:p.Asp17Asn
ENST00000587977.5:c.*146G>A	ENSP00000466587.1:n.*146G>A
ENST00000587982.5:n.273+304G>A
ENST00000588372.5:c.49G>A	ENSP00000468764.1:p.Asp17Asn
ENST00000588594.5:c.*76+304G>A	ENSP00000465366.1:n.*76+304G>A
ENST00000590016.5:c.466G>A	ENSP00000466399.1:p.Asp156Asn
ENST00000590631.1:c.-51-581G>A	ENSP00000465033.1:n.-51-581G>A
ENST00000591723.5:c.-52+304G>A	ENSP00000467986.1:n.-52+304G>A
ENST00000592181.1:c.49G>A	ENSP00000464799.1:p.Asp17Asn
ENST00000592430.5:n.375G>A
ENST00000592577.5:c.412G>A	ENSP00000466839.1:p.Asp138Asn
ENST00000592850.5:c.346-581G>A
ENST00000592928.2:n.167-581G>A
ENST00000593039.5:c.4-581G>A	ENSP00000466834.1:n.4-581G>A
NM_001142571.1:c.466G>A	NP_001136043.1:p.Asp156Asn
NM_002878.3:c.406G>A , LRG_516t1:c.406G>A	NP_002869.3:p.Asp136Asn
NM_133629.2:c.145-581G>A	NP_598332.1:n.145-581G>A
NR_037711.1:n.543G>A
NR_037712.1:n.482+304G>A
NR_037714.1:n.233-581G>A
NM_001142571.2:c.466G>A	NP_001136043.1:p.Asp156Asn
NM_133629.3:c.145-581G>A	NP_598332.1:n.145-581G>A
NR_037711.2:n.432G>A
NR_037712.2:n.371+304G>A
NM_002878.4:c.406G>A MANE Select	NP_002869.3:p.Asp136Asn