Canonical Allele Identifier: CA2622601871

Gene: BRCA2

Linked Data

• gnomAD v4: 13-32379706-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32379708dup , CM000675.2:g.32379708dup	GRCh38
NC_000013.10:g.32953845dup , CM000675.1:g.32953845dup	GRCh37
NC_000013.9:g.31851845dup	NCBI36
NG_012772.3:g.69229dup , LRG_293:g.69229dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8954-42dup	ENSP00000434898.2:n.8954-42dup
ENST00000528762.2:c.*321-42dup	ENSP00000433168.2:n.*321-42dup
ENST00000530893.7:c.8585-42dup	ENSP00000499438.2:n.8585-42dup
ENST00000665585.2:c.*516-42dup	ENSP00000499570.2:n.*516-42dup
ENST00000666593.2:c.8954-42dup	ENSP00000499256.2:n.8954-42dup
ENST00000700202.2:c.8954-93dup	ENSP00000514856.2:n.8954-93dup
ENST00000700202.1:c.1421-93dup	ENSP00000514856.1:n.1421-93dup
ENST00000700203.1:n.1081-42dup
ENST00000380152.8:c.8954-42dup MANE Select	ENSP00000369497.3:n.8954-42dup
ENST00000544455.6:c.8954-42dup	ENSP00000439902.1:n.8954-42dup
ENST00000614259.2:c.8962-42dup	ENSP00000506251.1:n.8962-42dup
ENST00000665585.1:c.1832-42dup
ENST00000680887.1:c.8954-42dup	ENSP00000505508.1:n.8954-42dup
ENST00000380152.7:c.8954-42dup	ENSP00000369497.3:n.8954-42dup
ENST00000544455.5:c.8954-42dup	ENSP00000439902.1:n.8954-42dup
NM_000059.3:c.8954-42dup , LRG_293t1:c.8954-42dup	NP_000050.2:n.8954-42dup
XM_011535203.1:c.8954-42dup	XP_011533505.1:n.8954-42dup
XM_011535204.1:c.8858-42dup	XP_011533506.1:n.8858-42dup
XM_011535205.1:c.8755-42dup	XP_011533507.1:n.8755-42dup
NM_000059.4:c.8954-42dup MANE Select	NP_000050.3:n.8954-42dup