Canonical Allele Identifier: CA399089198

Gene: RAD51D

Linked Data

• dbSNP Id: rs767981911
• MyVariant Identifiers: chr17:g.33434032G>C (hg19) ; chr17:g.35107013G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35107013G>C , CM000679.2:g.35107013G>C	GRCh38
NC_000017.10:g.33434032G>C , CM000679.1:g.33434032G>C	GRCh37
NC_000017.9:g.30458145G>C	NCBI36
NG_031858.1:g.17857C>G , LRG_516:g.17857C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.345+353C>G	ENSP00000468273.3:n.345+353C>G
ENST00000587405.6:c.98C>G	ENSP00000466478.2:p.Ala33Gly
ENST00000590016.6:c.515C>G	ENSP00000466399.1:p.Ala172Gly
ENST00000590631.2:n.437-532C>G
ENST00000592577.6:c.98C>G	ENSP00000466839.2:p.Ala33Gly
ENST00000345365.11:c.455C>G MANE Select	ENSP00000338790.6:p.Ala152Gly
ENST00000335858.11:c.145-532C>G	ENSP00000338408.6:n.145-532C>G
ENST00000345365.10:c.455C>G	ENSP00000338790.6:p.Ala152Gly
ENST00000394589.8:c.455C>G	ENSP00000378090.4:p.Ala152Gly
ENST00000415064.6:n.605C>G
ENST00000460118.6:c.-77C>G	ENSP00000464356.2:n.-77C>G
ENST00000585343.5:c.537C>G
ENST00000585947.5:n.351C>G
ENST00000585982.5:n.500+353C>G
ENST00000586044.5:c.*186C>G	ENSP00000465584.1:n.*186C>G
ENST00000586186.2:c.248+353C>G
ENST00000586210.5:c.*49C>G	ENSP00000465612.1:n.*49C>G
ENST00000587405.5:c.98C>G	ENSP00000466478.1:p.Ala33Gly
ENST00000587977.5:c.*195C>G	ENSP00000466587.1:n.*195C>G
ENST00000587982.5:n.273+353C>G
ENST00000588372.5:c.98C>G	ENSP00000468764.1:p.Ala33Gly
ENST00000588594.5:c.*76+353C>G	ENSP00000465366.1:n.*76+353C>G
ENST00000590016.5:c.515C>G	ENSP00000466399.1:p.Ala172Gly
ENST00000590631.1:c.-51-532C>G	ENSP00000465033.1:n.-51-532C>G
ENST00000591723.5:c.-52+353C>G	ENSP00000467986.1:n.-52+353C>G
ENST00000592181.1:c.98C>G	ENSP00000464799.1:p.Ala33Gly
ENST00000592430.5:n.424C>G
ENST00000592577.5:c.461C>G	ENSP00000466839.1:p.Ala154Gly
ENST00000592850.5:c.346-532C>G
ENST00000592928.2:n.167-532C>G
ENST00000593039.5:c.4-532C>G	ENSP00000466834.1:n.4-532C>G
NM_001142571.1:c.515C>G	NP_001136043.1:p.Ala172Gly
NM_002878.3:c.455C>G , LRG_516t1:c.455C>G	NP_002869.3:p.Ala152Gly
NM_133629.2:c.145-532C>G	NP_598332.1:n.145-532C>G
NR_037711.1:n.592C>G
NR_037712.1:n.482+353C>G
NR_037714.1:n.233-532C>G
NM_001142571.2:c.515C>G	NP_001136043.1:p.Ala172Gly
NM_133629.3:c.145-532C>G	NP_598332.1:n.145-532C>G
NR_037711.2:n.481C>G
NR_037712.2:n.371+353C>G
NM_002878.4:c.455C>G MANE Select	NP_002869.3:p.Ala152Gly