Canonical Allele Identifier: CA2622572518
Gene: BRCA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32362414_32362415del , CM000675.2:g.32362414_32362415del GRCh38
NC_000013.10:g.32936551_32936552del , CM000675.1:g.32936551_32936552del GRCh37
NC_000013.9:g.31834551_31834552del NCBI36
NG_012772.3:g.51935_51936del , LRG_293:g.51935_51936del

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.7806-109_7806-108del ENSP00000434898.2:n.7806-109_7806-108del
ENST00000528762.2:c.7806-109_7806-108del ENSP00000433168.2:n.7806-109_7806-108del
ENST00000530893.7:c.7437-109_7437-108del ENSP00000499438.2:n.7437-109_7437-108del
ENST00000665585.2:c.7806-109_7806-108del ENSP00000499570.2:n.7806-109_7806-108del
ENST00000666593.2:c.7806-109_7806-108del ENSP00000499256.2:n.7806-109_7806-108del
ENST00000700202.2:c.7806-109_7806-108del ENSP00000514856.2:n.7806-109_7806-108del
ENST00000700202.1:c.273-109_273-108del ENSP00000514856.1:n.273-109_273-108del
ENST00000380152.8:c.7806-109_7806-108del MANE Select ENSP00000369497.3:n.7806-109_7806-108del
ENST00000544455.6:c.7806-109_7806-108del ENSP00000439902.1:n.7806-109_7806-108del
ENST00000614259.2:c.7806-101_7806-100del ENSP00000506251.1:n.7806-101_7806-100del
ENST00000665585.1:c.371-109_371-108del
ENST00000680887.1:c.7806-109_7806-108del ENSP00000505508.1:n.7806-109_7806-108del
ENST00000380152.7:c.7806-109_7806-108del ENSP00000369497.3:n.7806-109_7806-108del
ENST00000544455.5:c.7806-109_7806-108del ENSP00000439902.1:n.7806-109_7806-108del
ENST00000614259.1:n.7806-101_7806-100del
NM_000059.3:c.7806-109_7806-108del , LRG_293t1:c.7806-109_7806-108del NP_000050.2:n.7806-109_7806-108del
XM_011535203.1:c.7806-109_7806-108del XP_011533505.1:n.7806-109_7806-108del
XM_011535204.1:c.7710-109_7710-108del XP_011533506.1:n.7710-109_7710-108del
XM_011535205.1:c.7806-109_7806-108del XP_011533507.1:n.7806-109_7806-108del
NM_000059.4:c.7806-109_7806-108del MANE Select NP_000050.3:n.7806-109_7806-108del