Canonical Allele Identifier: CA2622602679

Gene: BRCA2

Linked Data

• gnomAD v4: 13-32398030-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398031del , CM000675.2:g.32398031del	GRCh38
NC_000013.10:g.32972168del , CM000675.1:g.32972168del	GRCh37
NC_000013.9:g.31870168del	NCBI36
NG_012772.3:g.87552del , LRG_293:g.87552del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*172-131del	ENSP00000434898.2:n.*172-131del
ENST00000528762.2:c.*1016-131del	ENSP00000433168.2:n.*1016-131del
ENST00000530893.7:c.9280-131del	ENSP00000499438.2:n.9280-131del
ENST00000665585.2:c.*1211-131del	ENSP00000499570.2:n.*1211-131del
ENST00000700202.2:c.9598-131del	ENSP00000514856.2:n.9598-131del
ENST00000700202.1:c.2065-131del	ENSP00000514856.1:n.2065-131del
ENST00000700203.1:n.1776-131del
ENST00000380152.8:c.9649-131del MANE Select	ENSP00000369497.3:n.9649-131del
ENST00000544455.6:c.9649-131del	ENSP00000439902.1:n.9649-131del
ENST00000614259.2:c.9657-131del	ENSP00000506251.1:n.9657-131del
ENST00000665585.1:c.2527-131del
ENST00000680887.1:c.9649-131del	ENSP00000505508.1:n.9649-131del
ENST00000380152.7:c.9649-131del	ENSP00000369497.3:n.9649-131del
ENST00000470094.1:c.732-131del
ENST00000533776.1:n.237-131del
ENST00000544455.5:c.9649-131del	ENSP00000439902.1:n.9649-131del
NM_000059.3:c.9649-131del , LRG_293t1:c.9649-131del	NP_000050.2:n.9649-131del
XM_011535203.1:c.9649-131del	XP_011533505.1:n.9649-131del
XM_011535204.1:c.9553-131del	XP_011533506.1:n.9553-131del
NM_000059.4:c.9649-131del MANE Select	NP_000050.3:n.9649-131del