Canonical Allele Identifier: CA268836766

Gene: RAD51

Linked Data

• dbSNP Id: rs772375783
• gnomAD v4: 15-40695292-G-T
• MyVariant Identifiers: chr15:g.40987490G>T (hg19) ; chr15:g.40695292G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40695292G>T , CM000677.2:g.40695292G>T	GRCh38
NC_000015.9:g.40987490G>T , CM000677.1:g.40987490G>T	GRCh37
NC_000015.8:g.38774782G>T	NCBI36
NG_012120.1:g.5132G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267868.8:c.-136G>T MANE Select	ENSP00000267868.3:n.-136G>T
ENST00000645673.2:c.-136G>T	ENSP00000493712.2:n.-136G>T
ENST00000267868.7:c.-136G>T	ENSP00000267868.3:n.-136G>T
ENST00000382643.7:c.-32G>T	ENSP00000372088.3:n.-32G>T
ENST00000423169.6:c.-136G>T	ENSP00000406602.2:n.-136G>T
ENST00000525066.5:c.-136G>T	ENSP00000431864.1:n.-136G>T
ENST00000527860.5:c.-3+472G>T	ENSP00000432759.1:n.-3+472G>T
ENST00000532743.5:c.-136G>T	ENSP00000433924.1:n.-136G>T
ENST00000557850.5:c.-136G>T	ENSP00000454176.1:n.-136G>T
NM_001164269.1:c.-32G>T	NP_001157741.1:n.-32G>T
NM_001164270.1:c.-136G>T	NP_001157742.1:n.-136G>T
NM_002875.4:c.-136G>T	NP_002866.2:n.-136G>T
NM_133487.3:c.-136G>T	NP_597994.3:n.-136G>T
XM_011521857.1:c.-3+472G>T	XP_011520159.1:n.-3+472G>T
XM_011521860.1:c.-32G>T	XP_011520162.1:n.-32G>T
XM_011521861.1:c.-3+472G>T	XP_011520163.1:n.-3+472G>T
XM_011521862.1:c.-390G>T	XP_011520164.1:n.-390G>T
XM_011521857.2:c.-3+472G>T	XP_011520159.1:n.-3+472G>T
XM_011521860.2:c.-32G>T	XP_011520162.1:n.-32G>T
XM_011521861.2:c.-3+472G>T	XP_011520163.1:n.-3+472G>T
XM_011521862.3:c.-390G>T	XP_011520164.1:n.-390G>T
NM_001164269.2:c.-32G>T	NP_001157741.1:n.-32G>T
NM_001164270.2:c.-136G>T	NP_001157742.1:n.-136G>T
NM_002875.5:c.-136G>T MANE Select	NP_002866.2:n.-136G>T
NM_133487.4:c.-136G>T	NP_597994.3:n.-136G>T