Canonical Allele Identifier: CA7241144

Gene: RAD51B

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67887027A>C , CM000676.2:g.67887027A>C	GRCh38
NC_000014.8:g.68353744A>C , CM000676.1:g.68353744A>C	GRCh37
NC_000014.7:g.67423497A>C	NCBI36
NG_023267.1:g.72236A>C
NG_023267.2:g.72249A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_133510.4:c.579A>C MANE Select	NP_598194.1:p.Glu193Asp
ENST00000471583.6:c.579A>C MANE Select	ENSP00000418859.1:p.Glu193Asp
NM_001321809.1:c.579A>C	NP_001308738.1:p.Glu193Asp
NM_001321809.2:c.579A>C	NP_001308738.1:p.Glu193Asp
NM_001321810.1:c.579A>C	NP_001308739.1:p.Glu193Asp
NM_001321810.2:c.579A>C	NP_001308739.1:p.Glu193Asp
NM_001321812.1:c.579A>C	NP_001308741.1:p.Glu193Asp
NM_001321814.1:c.579A>C	NP_001308743.1:p.Glu193Asp
NM_001321814.2:c.579A>C	NP_001308743.1:p.Glu193Asp
NM_001321815.1:c.465A>C	NP_001308744.1:p.Glu155Asp
NM_001321817.1:c.222A>C	NP_001308746.1:p.Glu74Asp
NM_001321817.2:c.222A>C	NP_001308746.1:p.Glu74Asp
NM_001321818.1:c.579A>C	NP_001308747.1:p.Glu193Asp
NM_001321818.2:c.579A>C	NP_001308747.1:p.Glu193Asp
NM_001321819.1:c.579A>C	NP_001308748.1:p.Glu193Asp
NM_001321821.1:c.579A>C	NP_001308750.1:p.Glu193Asp
NM_001321821.2:c.579A>C	NP_001308750.1:p.Glu193Asp
NM_002877.5:c.579A>C	NP_002868.1:p.Glu193Asp
NM_002877.6:c.579A>C	NP_002868.1:p.Glu193Asp
NM_133509.3:c.579A>C	NP_598193.2:p.Glu193Asp
NM_133509.4:c.579A>C	NP_598193.2:p.Glu193Asp
NM_133509.5:c.579A>C	NP_598193.2:p.Glu193Asp
NM_133510.3:c.579A>C	NP_598194.1:p.Glu193Asp
ENST00000390683.7:c.579A>C	ENSP00000375101.4:p.Glu193Asp
ENST00000460526.6:c.579A>C	ENSP00000518559.1:p.Glu193Asp
ENST00000471583.5:c.579A>C	ENSP00000418859.1:p.Glu193Asp
ENST00000474051.1:n.263A>C
ENST00000479335.5:c.*350A>C	ENSP00000417408.1:n.*350A>C
ENST00000487270.5:c.579A>C	ENSP00000419471.1:p.Glu193Asp
ENST00000487861.5:c.579A>C	ENSP00000419881.1:p.Glu193Asp
ENST00000488612.5:c.579A>C	ENSP00000420061.1:p.Glu193Asp
ENST00000492236.5:n.109A>C
ENST00000497460.5:n.39A>C
ENST00000553595.5:n.235A>C
ENST00000553734.5:n.332A>C
ENST00000555907.5:n.430A>C
ENST00000711050.1:n.623A>C
XM_005267963.2:c.579A>C	XP_005268020.1:p.Glu193Asp
XM_011537047.1:c.579A>C	XP_011535349.1:p.Glu193Asp
XM_011537048.1:c.579A>C	XP_011535350.1:p.Glu193Asp
XM_011537049.1:c.579A>C	XP_011535351.1:p.Glu193Asp
XM_011537050.1:c.579A>C	XP_011535352.1:p.Glu193Asp
XM_011537050.3:c.579A>C	XP_011535352.1:p.Glu193Asp
XM_011537051.1:c.579A>C	XP_011535353.1:p.Glu193Asp
XM_017021545.2:c.579A>C	XP_016877034.1:p.Glu193Asp
XM_017021546.1:c.276A>C	XP_016877035.1:p.Glu92Asp
XM_017021547.1:c.222A>C	XP_016877036.1:p.Glu74Asp
XR_943503.1:n.656A>C