Canonical Allele Identifier: CA954697208
Gene: BRCA2 HGNC NCBI

Linked Data

dbSNP Id: rs2072704613

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32357283_32357284del , CM000675.2:g.32357283_32357284del GRCh38
NC_000013.10:g.32931420_32931421del , CM000675.1:g.32931420_32931421del GRCh37
NC_000013.9:g.31829420_31829421del NCBI36
NG_012772.3:g.46804_46805del , LRG_293:g.46804_46805del

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.7618-459_7618-458del ENSP00000434898.2:n.7618-459_7618-458del
ENST00000528762.2:c.7618-459_7618-458del ENSP00000433168.2:n.7618-459_7618-458del
ENST00000530893.7:c.7249-459_7249-458del ENSP00000499438.2:n.7249-459_7249-458del
ENST00000665585.2:c.7618-459_7618-458del ENSP00000499570.2:n.7618-459_7618-458del
ENST00000666593.2:c.7618-459_7618-458del ENSP00000499256.2:n.7618-459_7618-458del
ENST00000700202.2:c.7618-459_7618-458del ENSP00000514856.2:n.7618-459_7618-458del
ENST00000700202.1:c.85-459_85-458del ENSP00000514856.1:n.85-459_85-458del
ENST00000380152.8:c.7618-459_7618-458del MANE Select ENSP00000369497.3:n.7618-459_7618-458del
ENST00000544455.6:c.7618-459_7618-458del ENSP00000439902.1:n.7618-459_7618-458del
ENST00000614259.2:c.7618-459_7618-458del ENSP00000506251.1:n.7618-459_7618-458del
ENST00000665585.1:c.183-459_183-458del
ENST00000680887.1:c.7618-459_7618-458del ENSP00000505508.1:n.7618-459_7618-458del
ENST00000380152.7:c.7618-459_7618-458del ENSP00000369497.3:n.7618-459_7618-458del
ENST00000544455.5:c.7618-459_7618-458del ENSP00000439902.1:n.7618-459_7618-458del
ENST00000614259.1:n.7618-459_7618-458del
NM_000059.3:c.7618-459_7618-458del , LRG_293t1:c.7618-459_7618-458del NP_000050.2:n.7618-459_7618-458del
XM_011535203.1:c.7618-459_7618-458del XP_011533505.1:n.7618-459_7618-458del
XM_011535204.1:c.7522-459_7522-458del XP_011533506.1:n.7522-459_7522-458del
XM_011535205.1:c.7618-459_7618-458del XP_011533507.1:n.7618-459_7618-458del
NM_000059.4:c.7618-459_7618-458del MANE Select NP_000050.3:n.7618-459_7618-458del