Canonical Allele Identifier: CA399086085

Gene: RAD51D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35100983C>G , CM000679.2:g.35100983C>G	GRCh38
NC_000017.10:g.33428002C>G , CM000679.1:g.33428002C>G	GRCh37
NC_000017.9:g.30452115C>G	NCBI36
NG_031858.1:g.23887G>C , LRG_516:g.23887G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_002878.4:c.957G>C MANE Select	NP_002869.3:p.Gln319His
ENST00000345365.11:c.957G>C MANE Select	ENSP00000338790.6:p.Gln319His
NM_001142571.1:c.1017G>C	NP_001136043.1:p.Gln339His
NM_001142571.2:c.1017G>C	NP_001136043.1:p.Gln339His
NM_002878.3:c.957G>C , LRG_516t1:c.957G>C	NP_002869.3:p.Gln319His
NM_133629.2:c.621G>C	NP_598332.1:p.Gln207His
NM_133629.3:c.621G>C	NP_598332.1:p.Gln207His
NR_037711.1:n.1094G>C
NR_037711.2:n.983G>C
NR_037712.1:n.959G>C
NR_037712.2:n.848G>C
NR_037714.1:n.655+218G>C
ENST00000335858.11:c.621G>C	ENSP00000338408.6:p.Gln207His
ENST00000345365.10:c.957G>C	ENSP00000338790.6:p.Gln319His
ENST00000394589.8:c.957G>C	ENSP00000378090.4:p.Gln319His
ENST00000460118.6:c.426G>C	ENSP00000464356.2:p.Gln142His
ENST00000586044.5:c.*688G>C	ENSP00000465584.1:n.*688G>C
ENST00000586186.3:c.822G>C	ENSP00000468273.3:p.Gln274His
ENST00000586210.5:c.*551G>C	ENSP00000465612.1:n.*551G>C
ENST00000587405.6:c.600G>C	ENSP00000466478.2:p.Gln200His
ENST00000587977.5:c.*697G>C	ENSP00000466587.1:n.*697G>C
ENST00000588372.5:c.*440G>C	ENSP00000468764.1:n.*440G>C
ENST00000588594.5:c.*553G>C	ENSP00000465366.1:n.*553G>C
ENST00000590016.5:c.1017G>C	ENSP00000466399.1:p.Gln339His
ENST00000590016.6:c.1017G>C	ENSP00000466399.1:p.Gln339His
ENST00000591723.5:c.372+218G>C	ENSP00000467986.1:n.372+218G>C
ENST00000592181.1:c.546+218G>C	ENSP00000464799.1:n.546+218G>C
ENST00000592577.6:c.600G>C	ENSP00000466839.2:p.Gln200His
ENST00000593039.5:c.426+218G>C	ENSP00000466834.1:n.426+218G>C