Canonical Allele Identifier: CA2144362661
Gene: RAD51B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.68564607_68564619delinsAGCCTTAACCCCG , CM000676.2:g.68564607_68564619delinsAGCCTTAACCCCG GRCh38
NC_000014.8:g.69031324_69031336delinsAGCCTTAACCCCG , CM000676.1:g.69031324_69031336delinsAGCCTTAACCCCG GRCh37
NC_000014.7:g.68101077_68101089delinsAGCCTTAACCCCG NCBI36
NG_023267.1:g.749816_749828delinsAGCCTTAACCCCG
NG_023267.2:g.749829_749841delinsAGCCTTAACCCCG

Transcript Alleles

HGVS Amino-acid change
ENST00000478014.5:n.383+96357_383+96369delinsAGCCTTAACCCCG
ENST00000487270.5:c.1037-29878_1037-29866delinsAGCCTTAACCCCG ENSP00000419471.1:n.1037-29878_1037-29866delinsAGCCTTAACCCCG
ENST00000487861.5:c.1037-46399_1037-46387delinsAGCCTTAACCCCG ENSP00000419881.1:n.1037-46399_1037-46387delinsAGCCTTAACCCCG
ENST00000488612.5:c.1037-86174_1037-86162delinsAGCCTTAACCCCG ENSP00000420061.1:n.1037-86174_1037-86162delinsAGCCTTAACCCCG
ENST00000553595.5:n.614-118330_614-118318delinsAGCCTTAACCCCG
ENST00000554244.5:n.487+989_487+1001delinsAGCCTTAACCCCG
ENST00000556251.1:n.63+18983_63+18995delinsAGCCTTAACCCCG
NM_133509.3:c.1037-29878_1037-29866delinsAGCCTTAACCCCG NP_598193.2:n.1037-29878_1037-29866delinsAGCCTTAACCCCG
XM_005267963.2:c.1036+96357_1036+96369delinsAGCCTTAACCCCG XP_005268020.1:n.1036+96357_1036+96369delinsAGCCTTAACCCCG
XM_011537047.1:c.1037-43289_1037-43277delinsAGCCTTAACCCCG XP_011535349.1:n.1037-43289_1037-43277delinsAGCCTTAACCCCG
XM_011537048.1:c.1037-46399_1037-46387delinsAGCCTTAACCCCG XP_011535350.1:n.1037-46399_1037-46387delinsAGCCTTAACCCCG
XM_011537049.1:c.*1053_*1065delinsAGCCTTAACCCCG XP_011535351.1:n.*1053_*1065delinsAGCCTTAACCCCG
XR_943503.1:n.1407+96357_1407+96369delinsAGCCTTAACCCCG
XR_943975.1:n.87+530_87+542delinsCGGGGTTAAGGCT
NM_001321809.1:c.1037-38056_1037-38044delinsAGCCTTAACCCCG NP_001308738.1:n.1037-38056_1037-38044delinsAGCCTTAACCCCG
NM_001321810.1:c.1037-38056_1037-38044delinsAGCCTTAACCCCG NP_001308739.1:n.1037-38056_1037-38044delinsAGCCTTAACCCCG
NM_001321815.1:c.923-46551_923-46539delinsAGCCTTAACCCCG NP_001308744.1:n.923-46551_923-46539delinsAGCCTTAACCCCG
NM_001321818.1:c.1036+96357_1036+96369delinsAGCCTTAACCCCG NP_001308747.1:n.1036+96357_1036+96369delinsAGCCTTAACCCCG
NM_001321821.1:c.1037-46399_1037-46387delinsAGCCTTAACCCCG NP_001308750.1:n.1037-46399_1037-46387delinsAGCCTTAACCCCG
XM_017021546.1:c.734-46399_734-46387delinsAGCCTTAACCCCG XP_016877035.1:n.734-46399_734-46387delinsAGCCTTAACCCCG
XM_017021547.1:c.680-46399_680-46387delinsAGCCTTAACCCCG XP_016877036.1:n.680-46399_680-46387delinsAGCCTTAACCCCG
XM_017021548.1:c.305-46399_305-46387delinsAGCCTTAACCCCG XP_016877037.1:n.305-46399_305-46387delinsAGCCTTAACCCCG
NM_133509.4:c.1037-29878_1037-29866delinsAGCCTTAACCCCG NP_598193.2:n.1037-29878_1037-29866delinsAGCCTTAACCCCG
NM_001321809.2:c.1037-38056_1037-38044delinsAGCCTTAACCCCG NP_001308738.1:n.1037-38056_1037-38044delinsAGCCTTAACCCCG
NM_001321810.2:c.1037-38056_1037-38044delinsAGCCTTAACCCCG NP_001308739.1:n.1037-38056_1037-38044delinsAGCCTTAACCCCG
NM_001321818.2:c.1036+96357_1036+96369delinsAGCCTTAACCCCG NP_001308747.1:n.1036+96357_1036+96369delinsAGCCTTAACCCCG
NM_001321821.2:c.1037-46399_1037-46387delinsAGCCTTAACCCCG NP_001308750.1:n.1037-46399_1037-46387delinsAGCCTTAACCCCG
NM_133509.5:c.1037-29878_1037-29866delinsAGCCTTAACCCCG NP_598193.2:n.1037-29878_1037-29866delinsAGCCTTAACCCCG