Canonical Allele Identifier: CA2082835693
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1017075
ClinVar RCV Id: RCV001316169
dbSNP Id: rs2072898775

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32379370_32379393del , CM000675.2:g.32379370_32379393del GRCh38
NC_000013.10:g.32953507_32953530del , CM000675.1:g.32953507_32953530del GRCh37
NC_000013.9:g.31851507_31851530del NCBI36
NG_012772.3:g.68891_68914del , LRG_293:g.68891_68914del

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.8808_8831del ENSP00000434898.2:p.Leu2936_Ile2944delins...
ENST00000528762.2:c.*175_*198del ENSP00000433168.2:n.*175_*198del
ENST00000530893.7:c.8439_8462del ENSP00000499438.2:p.Leu2813_Ile2821delins...
ENST00000665585.2:c.*370_*393del ENSP00000499570.2:n.*370_*393del
ENST00000666593.2:c.8808_8831del ENSP00000499256.2:p.Leu2936_Ile2944delins...
ENST00000700202.2:c.8808_8831del ENSP00000514856.2:p.Leu2936_Ile2944delins...
ENST00000700202.1:c.1275_1298del ENSP00000514856.1:p.Leu425_Ile433delinsPh...
ENST00000700203.1:n.935_958del
ENST00000380152.8:c.8808_8831del MANE Select ENSP00000369497.3:p.Leu2936_Ile2944delins...
ENST00000544455.6:c.8808_8831del ENSP00000439902.1:p.Leu2936_Ile2944delins...
ENST00000614259.2:c.8816_8839del ENSP00000506251.1:n.8816_8839del
ENST00000665585.1:c.1686_1709del
ENST00000680887.1:c.8808_8831del ENSP00000505508.1:p.Leu2936_Ile2944delins...
ENST00000380152.7:c.8808_8831del ENSP00000369497.3:p.Leu2936_Ile2944delins...
ENST00000528762.1:c.370_393del ENSP00000433168.1:n.370_393del
ENST00000544455.5:c.8808_8831del ENSP00000439902.1:p.Leu2936_Ile2944delins...
NM_000059.3:c.8808_8831del , LRG_293t1:c.8808_8831del NP_000050.2:p.Leu2936_Ile2944delinsPhe
XM_011535203.1:c.8808_8831del XP_011533505.1:p.Leu2936_Ile2944delinsPhe...
XM_011535204.1:c.8712_8735del XP_011533506.1:p.Leu2904_Ile2912delinsPhe...
XM_011535205.1:c.8755-380_8755-357del XP_011533507.1:n.8755-380_8755-357del
NM_000059.4:c.8808_8831del MANE Select NP_000050.3:p.Leu2936_Ile2944delinsPhe