Canonical Allele Identifier: CA954698194
Gene: BRCA2 HGNC NCBI

Linked Data

dbSNP Id: rs2072872989

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32376540_32376542del , CM000675.2:g.32376540_32376542del GRCh38
NC_000013.10:g.32950677_32950679del , CM000675.1:g.32950677_32950679del GRCh37
NC_000013.9:g.31848677_31848679del NCBI36
NG_012772.3:g.66061_66063del , LRG_293:g.66061_66063del

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.8633-130_8633-128del ENSP00000434898.2:n.8633-130_8633-128del
ENST00000528762.2:c.8697-130_8697-128del ENSP00000433168.2:n.8697-130_8697-128del
ENST00000530893.7:c.8264-130_8264-128del ENSP00000499438.2:n.8264-130_8264-128del
ENST00000665585.2:c.*195-130_*195-128del ENSP00000499570.2:n.*195-130_*195-128del
ENST00000666593.2:c.8633-130_8633-128del ENSP00000499256.2:n.8633-130_8633-128del
ENST00000700202.2:c.8633-130_8633-128del ENSP00000514856.2:n.8633-130_8633-128del
ENST00000700202.1:c.1100-130_1100-128del ENSP00000514856.1:n.1100-130_1100-128del
ENST00000700203.1:n.630_632del
ENST00000380152.8:c.8633-130_8633-128del MANE Select ENSP00000369497.3:n.8633-130_8633-128del
ENST00000544455.6:c.8633-130_8633-128del ENSP00000439902.1:n.8633-130_8633-128del
ENST00000614259.2:c.8641-130_8641-128del ENSP00000506251.1:n.8641-130_8641-128del
ENST00000665585.1:c.1511-130_1511-128del
ENST00000680887.1:c.8633-130_8633-128del ENSP00000505508.1:n.8633-130_8633-128del
ENST00000380152.7:c.8633-130_8633-128del ENSP00000369497.3:n.8633-130_8633-128del
ENST00000528762.1:c.195-130_195-128del ENSP00000433168.1:n.195-130_195-128del
ENST00000544455.5:c.8633-130_8633-128del ENSP00000439902.1:n.8633-130_8633-128del
NM_000059.3:c.8633-130_8633-128del , LRG_293t1:c.8633-130_8633-128del NP_000050.2:n.8633-130_8633-128del
XM_011535203.1:c.8633-130_8633-128del XP_011533505.1:n.8633-130_8633-128del
XM_011535204.1:c.8537-130_8537-128del XP_011533506.1:n.8537-130_8537-128del
XM_011535205.1:c.8633-130_8633-128del XP_011533507.1:n.8633-130_8633-128del
NM_000059.4:c.8633-130_8633-128del MANE Select NP_000050.3:n.8633-130_8633-128del