Canonical Allele Identifier: CA7240992
Gene: RAD51B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.67835058dup , CM000676.2:g.67835058dup GRCh38
NC_000014.8:g.68301775dup , CM000676.1:g.68301775dup GRCh37
NC_000014.7:g.67371528dup NCBI36
NG_023267.1:g.20267dup
NG_023267.2:g.20280dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000460526.6:c.199-22dup ENSP00000518559.1:n.199-22dup
ENST00000711050.1:n.243-22dup
ENST00000471583.6:c.199-22dup MANE Select ENSP00000418859.1:n.199-22dup
ENST00000390683.7:c.199-22dup ENSP00000375101.4:n.199-22dup
ENST00000471583.5:c.199-22dup ENSP00000418859.1:n.199-22dup
ENST00000479335.5:c.199-22dup ENSP00000417408.1:n.199-22dup
ENST00000485181.5:c.199-22dup ENSP00000417948.1:n.199-22dup
ENST00000487270.5:c.199-22dup ENSP00000419471.1:n.199-22dup
ENST00000487861.5:c.199-22dup ENSP00000419881.1:n.199-22dup
ENST00000488612.5:c.199-22dup ENSP00000420061.1:n.199-22dup
ENST00000553334.1:c.199-22dup ENSP00000452044.1:n.199-22dup
NM_002877.5:c.199-22dup NP_002868.1:n.199-22dup
NM_133509.3:c.199-22dup NP_598193.2:n.199-22dup
NM_133510.3:c.199-22dup NP_598194.1:n.199-22dup
XM_005267963.2:c.199-22dup XP_005268020.1:n.199-22dup
XM_011537047.1:c.199-22dup XP_011535349.1:n.199-22dup
XM_011537048.1:c.199-22dup XP_011535350.1:n.199-22dup
XM_011537049.1:c.199-22dup XP_011535351.1:n.199-22dup
XM_011537050.1:c.199-22dup XP_011535352.1:n.199-22dup
XM_011537051.1:c.199-22dup XP_011535353.1:n.199-22dup
XR_943503.1:n.276-22dup
NM_001321809.1:c.199-22dup NP_001308738.1:n.199-22dup
NM_001321810.1:c.199-22dup NP_001308739.1:n.199-22dup
NM_001321812.1:c.199-22dup NP_001308741.1:n.199-22dup
NM_001321814.1:c.199-22dup NP_001308743.1:n.199-22dup
NM_001321815.1:c.85-22dup NP_001308744.1:n.85-22dup
NM_001321817.1:c.-257-22dup NP_001308746.1:n.-257-22dup
NM_001321818.1:c.199-22dup NP_001308747.1:n.199-22dup
NM_001321819.1:c.199-22dup NP_001308748.1:n.199-22dup
NM_001321821.1:c.199-22dup NP_001308750.1:n.199-22dup
XM_011537050.3:c.199-22dup XP_011535352.1:n.199-22dup
XM_017021545.2:c.199-22dup XP_016877034.1:n.199-22dup
NM_001321817.2:c.-257-22dup NP_001308746.1:n.-257-22dup
NM_002877.6:c.199-22dup NP_002868.1:n.199-22dup
NM_133509.4:c.199-22dup NP_598193.2:n.199-22dup
NM_133510.4:c.199-22dup MANE Select NP_598194.1:n.199-22dup
NM_001321809.2:c.199-22dup NP_001308738.1:n.199-22dup
NM_001321810.2:c.199-22dup NP_001308739.1:n.199-22dup
NM_001321814.2:c.199-22dup NP_001308743.1:n.199-22dup
NM_001321818.2:c.199-22dup NP_001308747.1:n.199-22dup
NM_001321821.2:c.199-22dup NP_001308750.1:n.199-22dup
NM_133509.5:c.199-22dup NP_598193.2:n.199-22dup