Canonical Allele Identifier: CA499731747

Gene: RAD51D

Linked Data

• MyVariant Identifiers: chr17:g.33434124T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35107105T>G , CM000679.2:g.35107105T>G	GRCh38
NC_000017.10:g.33434124T>G , CM000679.1:g.33434124T>G	GRCh37
NC_000017.9:g.30458237T>G	NCBI36
NG_031858.1:g.17765A>C , LRG_516:g.17765A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.345+261A>C	ENSP00000468273.3:n.345+261A>C
ENST00000587405.6:c.6A>C	ENSP00000466478.2:p.Ala2=
ENST00000590016.6:c.423A>C	ENSP00000466399.1:p.Ala141=
ENST00000590631.2:n.437-624A>C
ENST00000592577.6:c.6A>C	ENSP00000466839.2:p.Ala2=
ENST00000345365.11:c.363A>C MANE Select	ENSP00000338790.6:p.Ala121=
ENST00000335858.11:c.145-624A>C	ENSP00000338408.6:n.145-624A>C
ENST00000345365.10:c.363A>C	ENSP00000338790.6:p.Ala121=
ENST00000394589.8:c.363A>C	ENSP00000378090.4:p.Ala121=
ENST00000415064.6:n.513A>C
ENST00000460118.6:c.-125-44A>C	ENSP00000464356.2:n.-125-44A>C
ENST00000585343.5:c.445A>C
ENST00000585947.5:n.259A>C
ENST00000585982.5:n.500+261A>C
ENST00000586044.5:c.*94A>C	ENSP00000465584.1:n.*94A>C
ENST00000586186.2:c.248+261A>C
ENST00000586210.5:c.281A>C	ENSP00000465612.1:p.Gln94Pro
ENST00000587405.5:c.6A>C	ENSP00000466478.1:p.Ala2=
ENST00000587977.5:c.*103A>C	ENSP00000466587.1:n.*103A>C
ENST00000587982.5:n.273+261A>C
ENST00000588372.5:c.6A>C	ENSP00000468764.1:p.Ala2=
ENST00000588594.5:c.*76+261A>C	ENSP00000465366.1:n.*76+261A>C
ENST00000590016.5:c.423A>C	ENSP00000466399.1:p.Ala141=
ENST00000590631.1:c.-51-624A>C	ENSP00000465033.1:n.-51-624A>C
ENST00000591723.5:c.-52+261A>C	ENSP00000467986.1:n.-52+261A>C
ENST00000592181.1:c.6A>C	ENSP00000464799.1:p.Ala2=
ENST00000592430.5:n.332A>C
ENST00000592577.5:c.369A>C	ENSP00000466839.1:p.Ala123=
ENST00000592850.5:c.346-624A>C
ENST00000592928.2:n.167-624A>C
ENST00000593039.5:c.4-624A>C	ENSP00000466834.1:n.4-624A>C
NM_001142571.1:c.423A>C	NP_001136043.1:p.Ala141=
NM_002878.3:c.363A>C , LRG_516t1:c.363A>C	NP_002869.3:p.Ala121=
NM_133629.2:c.145-624A>C	NP_598332.1:n.145-624A>C
NR_037711.1:n.500A>C
NR_037712.1:n.482+261A>C
NR_037714.1:n.233-624A>C
NM_001142571.2:c.423A>C	NP_001136043.1:p.Ala141=
NM_133629.3:c.145-624A>C	NP_598332.1:n.145-624A>C
NR_037711.2:n.389A>C
NR_037712.2:n.371+261A>C
NM_002878.4:c.363A>C MANE Select	NP_002869.3:p.Ala121=