Canonical Allele Identifier: CA499731695

Gene: RAD51D

Linked Data

• dbSNP Id: rs2142432832
• MyVariant Identifiers: chr17:g.33434055G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35107036G>C , CM000679.2:g.35107036G>C	GRCh38
NC_000017.10:g.33434055G>C , CM000679.1:g.33434055G>C	GRCh37
NC_000017.9:g.30458168G>C	NCBI36
NG_031858.1:g.17834C>G , LRG_516:g.17834C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586186.3:c.345+330C>G	ENSP00000468273.3:n.345+330C>G
ENST00000587405.6:c.75C>G	ENSP00000466478.2:p.Ser25=
ENST00000590016.6:c.492C>G	ENSP00000466399.1:p.Ser164=
ENST00000590631.2:n.437-555C>G
ENST00000592577.6:c.75C>G	ENSP00000466839.2:p.Ser25=
ENST00000345365.11:c.432C>G MANE Select	ENSP00000338790.6:p.Ser144=
ENST00000335858.11:c.145-555C>G	ENSP00000338408.6:n.145-555C>G
ENST00000345365.10:c.432C>G	ENSP00000338790.6:p.Ser144=
ENST00000394589.8:c.432C>G	ENSP00000378090.4:p.Ser144=
ENST00000415064.6:n.582C>G
ENST00000460118.6:c.-100C>G	ENSP00000464356.2:n.-100C>G
ENST00000585343.5:c.514C>G
ENST00000585947.5:n.328C>G
ENST00000585982.5:n.500+330C>G
ENST00000586044.5:c.*163C>G	ENSP00000465584.1:n.*163C>G
ENST00000586186.2:c.248+330C>G
ENST00000586210.5:c.*26C>G	ENSP00000465612.1:n.*26C>G
ENST00000587405.5:c.75C>G	ENSP00000466478.1:p.Ser25=
ENST00000587977.5:c.*172C>G	ENSP00000466587.1:n.*172C>G
ENST00000587982.5:n.273+330C>G
ENST00000588372.5:c.75C>G	ENSP00000468764.1:p.Ser25=
ENST00000588594.5:c.*76+330C>G	ENSP00000465366.1:n.*76+330C>G
ENST00000590016.5:c.492C>G	ENSP00000466399.1:p.Ser164=
ENST00000590631.1:c.-51-555C>G	ENSP00000465033.1:n.-51-555C>G
ENST00000591723.5:c.-52+330C>G	ENSP00000467986.1:n.-52+330C>G
ENST00000592181.1:c.75C>G	ENSP00000464799.1:p.Ser25=
ENST00000592430.5:n.401C>G
ENST00000592577.5:c.438C>G	ENSP00000466839.1:p.Ser146=
ENST00000592850.5:c.346-555C>G
ENST00000592928.2:n.167-555C>G
ENST00000593039.5:c.4-555C>G	ENSP00000466834.1:n.4-555C>G
NM_001142571.1:c.492C>G	NP_001136043.1:p.Ser164=
NM_002878.3:c.432C>G , LRG_516t1:c.432C>G	NP_002869.3:p.Ser144=
NM_133629.2:c.145-555C>G	NP_598332.1:n.145-555C>G
NR_037711.1:n.569C>G
NR_037712.1:n.482+330C>G
NR_037714.1:n.233-555C>G
NM_001142571.2:c.492C>G	NP_001136043.1:p.Ser164=
NM_133629.3:c.145-555C>G	NP_598332.1:n.145-555C>G
NR_037711.2:n.458C>G
NR_037712.2:n.371+330C>G
NM_002878.4:c.432C>G MANE Select	NP_002869.3:p.Ser144=