Canonical Allele Identifier: CA499728599

Gene: RAD51D

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35101004C>G , CM000679.2:g.35101004C>G	GRCh38
NC_000017.10:g.33428023C>G , CM000679.1:g.33428023C>G	GRCh37
NC_000017.9:g.30452136C>G	NCBI36
NG_031858.1:g.23866G>C , LRG_516:g.23866G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_002878.4:c.936G>C MANE Select	NP_002869.3:p.Gly312=
ENST00000345365.11:c.936G>C MANE Select	ENSP00000338790.6:p.Gly312=
NM_001142571.1:c.996G>C	NP_001136043.1:p.Gly332=
NM_001142571.2:c.996G>C	NP_001136043.1:p.Gly332=
NM_002878.3:c.936G>C , LRG_516t1:c.936G>C	NP_002869.3:p.Gly312=
NM_133629.2:c.600G>C	NP_598332.1:p.Gly200=
NM_133629.3:c.600G>C	NP_598332.1:p.Gly200=
NR_037711.1:n.1073G>C
NR_037711.2:n.962G>C
NR_037712.1:n.938G>C
NR_037712.2:n.827G>C
NR_037714.1:n.655+197G>C
ENST00000335858.11:c.600G>C	ENSP00000338408.6:p.Gly200=
ENST00000345365.10:c.936G>C	ENSP00000338790.6:p.Gly312=
ENST00000394589.8:c.936G>C	ENSP00000378090.4:p.Gly312=
ENST00000460118.6:c.405G>C	ENSP00000464356.2:p.Gly135=
ENST00000586044.5:c.*667G>C	ENSP00000465584.1:n.*667G>C
ENST00000586186.3:c.801G>C	ENSP00000468273.3:p.Gly267=
ENST00000586210.5:c.*530G>C	ENSP00000465612.1:n.*530G>C
ENST00000587405.6:c.579G>C	ENSP00000466478.2:p.Gly193=
ENST00000587977.5:c.*676G>C	ENSP00000466587.1:n.*676G>C
ENST00000588372.5:c.*419G>C	ENSP00000468764.1:n.*419G>C
ENST00000588594.5:c.*532G>C	ENSP00000465366.1:n.*532G>C
ENST00000590016.5:c.996G>C	ENSP00000466399.1:p.Gly332=
ENST00000590016.6:c.996G>C	ENSP00000466399.1:p.Gly332=
ENST00000591723.5:c.372+197G>C	ENSP00000467986.1:n.372+197G>C
ENST00000592181.1:c.546+197G>C	ENSP00000464799.1:n.546+197G>C
ENST00000592577.6:c.579G>C	ENSP00000466839.2:p.Gly193=
ENST00000593039.5:c.426+197G>C	ENSP00000466834.1:n.426+197G>C