Canonical Allele Identifier: CA954697720

Gene: BRCA2

Linked Data

• gnomAD v3: 13-32376181-C-CTT
• gnomAD v4: 13-32376181-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32376193_32376194dup , CM000675.2:g.32376193_32376194dup	GRCh38
NC_000013.10:g.32950330_32950331dup , CM000675.1:g.32950330_32950331dup	GRCh37
NC_000013.9:g.31848330_31848331dup	NCBI36
NG_012772.3:g.65714_65715dup , LRG_293:g.65714_65715dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8633-477_8633-476dup	ENSP00000434898.2:n.8633-477_8633-476dup
ENST00000528762.2:c.8697-477_8697-476dup	ENSP00000433168.2:n.8697-477_8697-476dup
ENST00000530893.7:c.8264-477_8264-476dup	ENSP00000499438.2:n.8264-477_8264-476dup
ENST00000665585.2:c.*195-477_*195-476dup	ENSP00000499570.2:n.*195-477_*195-476dup
ENST00000666593.2:c.8633-477_8633-476dup	ENSP00000499256.2:n.8633-477_8633-476dup
ENST00000700202.2:c.8633-477_8633-476dup	ENSP00000514856.2:n.8633-477_8633-476dup
ENST00000700202.1:c.1100-477_1100-476dup	ENSP00000514856.1:n.1100-477_1100-476dup
ENST00000700203.1:n.283_284dup
ENST00000380152.8:c.8633-477_8633-476dup MANE Select	ENSP00000369497.3:n.8633-477_8633-476dup
ENST00000544455.6:c.8633-477_8633-476dup	ENSP00000439902.1:n.8633-477_8633-476dup
ENST00000614259.2:c.8641-477_8641-476dup	ENSP00000506251.1:n.8641-477_8641-476dup
ENST00000665585.1:c.1511-477_1511-476dup
ENST00000680887.1:c.8633-477_8633-476dup	ENSP00000505508.1:n.8633-477_8633-476dup
ENST00000380152.7:c.8633-477_8633-476dup	ENSP00000369497.3:n.8633-477_8633-476dup
ENST00000528762.1:c.195-477_195-476dup	ENSP00000433168.1:n.195-477_195-476dup
ENST00000544455.5:c.8633-477_8633-476dup	ENSP00000439902.1:n.8633-477_8633-476dup
NM_000059.3:c.8633-477_8633-476dup , LRG_293t1:c.8633-477_8633-476dup	NP_000050.2:n.8633-477_8633-476dup
XM_011535203.1:c.8633-477_8633-476dup	XP_011533505.1:n.8633-477_8633-476dup
XM_011535204.1:c.8537-477_8537-476dup	XP_011533506.1:n.8537-477_8537-476dup
XM_011535205.1:c.8633-477_8633-476dup	XP_011533507.1:n.8633-477_8633-476dup
NM_000059.4:c.8633-477_8633-476dup MANE Select	NP_000050.3:n.8633-477_8633-476dup