Canonical Allele Identifier: CA399089284

Gene: RAD51D

Linked Data

• dbSNP Id: rs768197423
• MyVariant Identifiers: chr17:g.33434080T>G (hg19) ; chr17:g.35107061T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35107061T>G , CM000679.2:g.35107061T>G	GRCh38
NC_000017.10:g.33434080T>G , CM000679.1:g.33434080T>G	GRCh37
NC_000017.9:g.30458193T>G	NCBI36
NG_031858.1:g.17809A>C , LRG_516:g.17809A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.345+305A>C	ENSP00000468273.3:n.345+305A>C
ENST00000587405.6:c.50A>C	ENSP00000466478.2:p.Asp17Ala
ENST00000590016.6:c.467A>C	ENSP00000466399.1:p.Asp156Ala
ENST00000590631.2:n.437-580A>C
ENST00000592577.6:c.50A>C	ENSP00000466839.2:p.Asp17Ala
ENST00000345365.11:c.407A>C MANE Select	ENSP00000338790.6:p.Asp136Ala
ENST00000335858.11:c.145-580A>C	ENSP00000338408.6:n.145-580A>C
ENST00000345365.10:c.407A>C	ENSP00000338790.6:p.Asp136Ala
ENST00000394589.8:c.407A>C	ENSP00000378090.4:p.Asp136Ala
ENST00000415064.6:n.557A>C
ENST00000460118.6:c.-125A>C	ENSP00000464356.2:n.-125A>C
ENST00000585343.5:c.489A>C
ENST00000585947.5:n.303A>C
ENST00000585982.5:n.500+305A>C
ENST00000586044.5:c.*138A>C	ENSP00000465584.1:n.*138A>C
ENST00000586186.2:c.248+305A>C
ENST00000586210.5:c.*1A>C	ENSP00000465612.1:n.*1A>C
ENST00000587405.5:c.50A>C	ENSP00000466478.1:p.Asp17Ala
ENST00000587977.5:c.*147A>C	ENSP00000466587.1:n.*147A>C
ENST00000587982.5:n.273+305A>C
ENST00000588372.5:c.50A>C	ENSP00000468764.1:p.Asp17Ala
ENST00000588594.5:c.*76+305A>C	ENSP00000465366.1:n.*76+305A>C
ENST00000590016.5:c.467A>C	ENSP00000466399.1:p.Asp156Ala
ENST00000590631.1:c.-51-580A>C	ENSP00000465033.1:n.-51-580A>C
ENST00000591723.5:c.-52+305A>C	ENSP00000467986.1:n.-52+305A>C
ENST00000592181.1:c.50A>C	ENSP00000464799.1:p.Asp17Ala
ENST00000592430.5:n.376A>C
ENST00000592577.5:c.413A>C	ENSP00000466839.1:p.Asp138Ala
ENST00000592850.5:c.346-580A>C
ENST00000592928.2:n.167-580A>C
ENST00000593039.5:c.4-580A>C	ENSP00000466834.1:n.4-580A>C
NM_001142571.1:c.467A>C	NP_001136043.1:p.Asp156Ala
NM_002878.3:c.407A>C , LRG_516t1:c.407A>C	NP_002869.3:p.Asp136Ala
NM_133629.2:c.145-580A>C	NP_598332.1:n.145-580A>C
NR_037711.1:n.544A>C
NR_037712.1:n.482+305A>C
NR_037714.1:n.233-580A>C
NM_001142571.2:c.467A>C	NP_001136043.1:p.Asp156Ala
NM_133629.3:c.145-580A>C	NP_598332.1:n.145-580A>C
NR_037711.2:n.433A>C
NR_037712.2:n.371+305A>C
NM_002878.4:c.407A>C MANE Select	NP_002869.3:p.Asp136Ala