Canonical Allele Identifier: CA399088502

Gene: RAD51D

Linked Data

• MyVariant Identifiers: chr17:g.33433405C>G (hg19) ; chr17:g.35106386C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35106386C>G , CM000679.2:g.35106386C>G	GRCh38
NC_000017.10:g.33433405C>G , CM000679.1:g.33433405C>G	GRCh37
NC_000017.9:g.30457518C>G	NCBI36
NG_031858.1:g.18484G>C , LRG_516:g.18484G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000586186.3:c.441G>C	ENSP00000468273.3:p.Gln147His
ENST00000587405.6:c.219G>C	ENSP00000466478.2:p.Gln73His
ENST00000590016.6:c.636G>C	ENSP00000466399.1:p.Gln212His
ENST00000590631.2:n.532G>C
ENST00000592577.6:c.219G>C	ENSP00000466839.2:p.Gln73His
ENST00000345365.11:c.576G>C MANE Select	ENSP00000338790.6:p.Gln192His
ENST00000335858.11:c.240G>C	ENSP00000338408.6:p.Gln80His
ENST00000345365.10:c.576G>C	ENSP00000338790.6:p.Gln192His
ENST00000394589.8:c.576G>C	ENSP00000378090.4:p.Gln192His
ENST00000415064.6:n.726G>C
ENST00000460118.6:c.45G>C	ENSP00000464356.2:p.Gln15His
ENST00000585947.5:n.472G>C
ENST00000585982.5:n.596G>C
ENST00000586044.5:c.*307G>C	ENSP00000465584.1:n.*307G>C
ENST00000586210.5:c.*170G>C	ENSP00000465612.1:n.*170G>C
ENST00000587405.5:c.219G>C	ENSP00000466478.1:p.Gln73His
ENST00000587977.5:c.*316G>C	ENSP00000466587.1:n.*316G>C
ENST00000587982.5:n.369G>C
ENST00000588372.5:c.219G>C	ENSP00000468764.1:p.Gln73His
ENST00000588594.5:c.*172G>C	ENSP00000465366.1:n.*172G>C
ENST00000590016.5:c.636G>C	ENSP00000466399.1:p.Gln212His
ENST00000590631.1:c.45G>C	ENSP00000465033.1:p.Gln15His
ENST00000591723.5:c.45G>C	ENSP00000467986.1:p.Gln15His
ENST00000592181.1:c.219G>C	ENSP00000464799.1:p.Gln73His
ENST00000592430.5:n.545G>C
ENST00000592577.5:c.582G>C	ENSP00000466839.1:p.Gln194His
ENST00000593039.5:c.99G>C	ENSP00000466834.1:p.Gln33His
NM_001142571.1:c.636G>C	NP_001136043.1:p.Gln212His
NM_002878.3:c.576G>C , LRG_516t1:c.576G>C	NP_002869.3:p.Gln192His
NM_133629.2:c.240G>C	NP_598332.1:p.Gln80His
NR_037711.1:n.713G>C
NR_037712.1:n.578G>C
NR_037714.1:n.328G>C
NM_001142571.2:c.636G>C	NP_001136043.1:p.Gln212His
NM_133629.3:c.240G>C	NP_598332.1:p.Gln80His
NR_037711.2:n.602G>C
NR_037712.2:n.467G>C
NM_002878.4:c.576G>C MANE Select	NP_002869.3:p.Gln192His