Canonical Allele Identifier: CA499731727

Gene: RAD51D

Linked Data

• dbSNP Id: rs2142433416
• MyVariant Identifiers: chr17:g.33434097T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35107078T>C , CM000679.2:g.35107078T>C	GRCh38
NC_000017.10:g.33434097T>C , CM000679.1:g.33434097T>C	GRCh37
NC_000017.9:g.30458210T>C	NCBI36
NG_031858.1:g.17792A>G , LRG_516:g.17792A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.345+288A>G	ENSP00000468273.3:n.345+288A>G
ENST00000587405.6:c.33A>G	ENSP00000466478.2:p.Gln11=
ENST00000590016.6:c.450A>G	ENSP00000466399.1:p.Gln150=
ENST00000590631.2:n.437-597A>G
ENST00000592577.6:c.33A>G	ENSP00000466839.2:p.Gln11=
ENST00000345365.11:c.390A>G MANE Select	ENSP00000338790.6:p.Gln130=
ENST00000335858.11:c.145-597A>G	ENSP00000338408.6:n.145-597A>G
ENST00000345365.10:c.390A>G	ENSP00000338790.6:p.Gln130=
ENST00000394589.8:c.390A>G	ENSP00000378090.4:p.Gln130=
ENST00000415064.6:n.540A>G
ENST00000460118.6:c.-125-17A>G	ENSP00000464356.2:n.-125-17A>G
ENST00000585343.5:c.472A>G
ENST00000585947.5:n.286A>G
ENST00000585982.5:n.500+288A>G
ENST00000586044.5:c.*121A>G	ENSP00000465584.1:n.*121A>G
ENST00000586186.2:c.248+288A>G
ENST00000586210.5:c.308A>G	ENSP00000465612.1:p.Lys103Arg
ENST00000587405.5:c.33A>G	ENSP00000466478.1:p.Gln11=
ENST00000587977.5:c.*130A>G	ENSP00000466587.1:n.*130A>G
ENST00000587982.5:n.273+288A>G
ENST00000588372.5:c.33A>G	ENSP00000468764.1:p.Gln11=
ENST00000588594.5:c.*76+288A>G	ENSP00000465366.1:n.*76+288A>G
ENST00000590016.5:c.450A>G	ENSP00000466399.1:p.Gln150=
ENST00000590631.1:c.-51-597A>G	ENSP00000465033.1:n.-51-597A>G
ENST00000591723.5:c.-52+288A>G	ENSP00000467986.1:n.-52+288A>G
ENST00000592181.1:c.33A>G	ENSP00000464799.1:p.Gln11=
ENST00000592430.5:n.359A>G
ENST00000592577.5:c.396A>G	ENSP00000466839.1:p.Gln132=
ENST00000592850.5:c.346-597A>G
ENST00000592928.2:n.167-597A>G
ENST00000593039.5:c.4-597A>G	ENSP00000466834.1:n.4-597A>G
NM_001142571.1:c.450A>G	NP_001136043.1:p.Gln150=
NM_002878.3:c.390A>G , LRG_516t1:c.390A>G	NP_002869.3:p.Gln130=
NM_133629.2:c.145-597A>G	NP_598332.1:n.145-597A>G
NR_037711.1:n.527A>G
NR_037712.1:n.482+288A>G
NR_037714.1:n.233-597A>G
NM_001142571.2:c.450A>G	NP_001136043.1:p.Gln150=
NM_133629.3:c.145-597A>G	NP_598332.1:n.145-597A>G
NR_037711.2:n.416A>G
NR_037712.2:n.371+288A>G
NM_002878.4:c.390A>G MANE Select	NP_002869.3:p.Gln130=