Canonical Allele Identifier: CA697349733

Gene: BRCA2

Linked Data

• dbSNP Id: rs1348074343
• MyVariant Identifiers: chr13:g.32929487_32929488insT (hg19) ; chr13:g.32355350_32355351insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32355351dup , CM000675.2:g.32355351dup	GRCh38
NC_000013.10:g.32929488dup , CM000675.1:g.32929488dup	GRCh37
NC_000013.9:g.31827488dup	NCBI36
NG_012772.3:g.44872dup , LRG_293:g.44872dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7435+63dup	ENSP00000434898.2:n.7435+63dup
ENST00000528762.2:c.7435+63dup	ENSP00000433168.2:n.7435+63dup
ENST00000530893.7:c.7066+63dup	ENSP00000499438.2:n.7066+63dup
ENST00000665585.2:c.7435+63dup	ENSP00000499570.2:n.7435+63dup
ENST00000666593.2:c.7435+63dup	ENSP00000499256.2:n.7435+63dup
ENST00000700202.2:c.7435+63dup	ENSP00000514856.2:n.7435+63dup
ENST00000380152.8:c.7435+63dup MANE Select	ENSP00000369497.3:n.7435+63dup
ENST00000544455.6:c.7435+63dup	ENSP00000439902.1:n.7435+63dup
ENST00000614259.2:c.7435+63dup	ENSP00000506251.1:n.7435+63dup
ENST00000680887.1:c.7435+63dup	ENSP00000505508.1:n.7435+63dup
ENST00000380152.7:c.7435+63dup	ENSP00000369497.3:n.7435+63dup
ENST00000544455.5:c.7435+63dup	ENSP00000439902.1:n.7435+63dup
ENST00000614259.1:n.7435+63dup
NM_000059.3:c.7435+63dup , LRG_293t1:c.7435+63dup	NP_000050.2:n.7435+63dup
XM_011535203.1:c.7435+63dup	XP_011533505.1:n.7435+63dup
XM_011535204.1:c.7339+63dup	XP_011533506.1:n.7339+63dup
XM_011535205.1:c.7435+63dup	XP_011533507.1:n.7435+63dup
NM_000059.4:c.7435+63dup MANE Select	NP_000050.3:n.7435+63dup