Canonical Allele Identifier: CA2144362608

Gene: RAD51B

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.68564480_68564483delinsCTTG , CM000676.2:g.68564480_68564483delinsCTTG	GRCh38
NC_000014.8:g.69031197_69031200delinsCTTG , CM000676.1:g.69031197_69031200delinsCTTG	GRCh37
NC_000014.7:g.68100950_68100953delinsCTTG	NCBI36
NG_023267.1:g.749689_749692delinsCTTG
NG_023267.2:g.749702_749705delinsCTTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000478014.5:n.383+96230_383+96233delinsCTTG
ENST00000487270.5:c.1037-30005_1037-30002delinsCTTG	ENSP00000419471.1:n.1037-30005_1037-30002delinsCTTG
ENST00000487861.5:c.1037-46526_1037-46523delinsCTTG	ENSP00000419881.1:n.1037-46526_1037-46523delinsCTTG
ENST00000488612.5:c.1037-86301_1037-86298delinsCTTG	ENSP00000420061.1:n.1037-86301_1037-86298delinsCTTG
ENST00000553595.5:n.614-118457_614-118454delinsCTTG
ENST00000554244.5:n.487+862_487+865delinsCTTG
ENST00000556251.1:n.63+18856_63+18859delinsCTTG
NM_133509.3:c.1037-30005_1037-30002delinsCTTG	NP_598193.2:n.1037-30005_1037-30002delinsCTTG
XM_005267963.2:c.1036+96230_1036+96233delinsCTTG	XP_005268020.1:n.1036+96230_1036+96233delinsCTTG
XM_011537047.1:c.1037-43416_1037-43413delinsCTTG	XP_011535349.1:n.1037-43416_1037-43413delinsCTTG
XM_011537048.1:c.1037-46526_1037-46523delinsCTTG	XP_011535350.1:n.1037-46526_1037-46523delinsCTTG
XM_011537049.1:c.*926_*929delinsCTTG	XP_011535351.1:n.*926_*929delinsCTTG
XR_943503.1:n.1407+96230_1407+96233delinsCTTG
XR_943975.1:n.87+666_87+669delinsCAAG
NM_001321809.1:c.1037-38183_1037-38180delinsCTTG	NP_001308738.1:n.1037-38183_1037-38180delinsCTTG
NM_001321810.1:c.1037-38183_1037-38180delinsCTTG	NP_001308739.1:n.1037-38183_1037-38180delinsCTTG
NM_001321815.1:c.923-46678_923-46675delinsCTTG	NP_001308744.1:n.923-46678_923-46675delinsCTTG
NM_001321818.1:c.1036+96230_1036+96233delinsCTTG	NP_001308747.1:n.1036+96230_1036+96233delinsCTTG
NM_001321821.1:c.1037-46526_1037-46523delinsCTTG	NP_001308750.1:n.1037-46526_1037-46523delinsCTTG
XM_017021546.1:c.734-46526_734-46523delinsCTTG	XP_016877035.1:n.734-46526_734-46523delinsCTTG
XM_017021547.1:c.680-46526_680-46523delinsCTTG	XP_016877036.1:n.680-46526_680-46523delinsCTTG
XM_017021548.1:c.305-46526_305-46523delinsCTTG	XP_016877037.1:n.305-46526_305-46523delinsCTTG
NM_133509.4:c.1037-30005_1037-30002delinsCTTG	NP_598193.2:n.1037-30005_1037-30002delinsCTTG
NM_001321809.2:c.1037-38183_1037-38180delinsCTTG	NP_001308738.1:n.1037-38183_1037-38180delinsCTTG
NM_001321810.2:c.1037-38183_1037-38180delinsCTTG	NP_001308739.1:n.1037-38183_1037-38180delinsCTTG
NM_001321818.2:c.1036+96230_1036+96233delinsCTTG	NP_001308747.1:n.1036+96230_1036+96233delinsCTTG
NM_001321821.2:c.1037-46526_1037-46523delinsCTTG	NP_001308750.1:n.1037-46526_1037-46523delinsCTTG
NM_133509.5:c.1037-30005_1037-30002delinsCTTG	NP_598193.2:n.1037-30005_1037-30002delinsCTTG