Canonical Allele Identifier: CA2082816731

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32371115_32371118delinsATGG , CM000675.2:g.32371115_32371118delinsATGG	GRCh38
NC_000013.10:g.32945252_32945255delinsATGG , CM000675.1:g.32945252_32945255delinsATGG	GRCh37
NC_000013.9:g.31843252_31843255delinsATGG	NCBI36
NG_012772.3:g.60636_60639delinsATGG , LRG_293:g.60636_60639delinsATGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8632+15_8632+18delinsATGG	ENSP00000434898.2:n.8632+15_8632+18delinsATGG
ENST00000528762.2:c.8632+15_8632+18delinsATGG	ENSP00000433168.2:n.8632+15_8632+18delinsATGG
ENST00000530893.7:c.8263+15_8263+18delinsATGG	ENSP00000499438.2:n.8263+15_8263+18delinsATGG
ENST00000665585.2:c.8632+15_8632+18delinsATGG	ENSP00000499570.2:n.8632+15_8632+18delinsATGG
ENST00000666593.2:c.8632+15_8632+18delinsATGG	ENSP00000499256.2:n.8632+15_8632+18delinsATGG
ENST00000700202.2:c.8632+15_8632+18delinsATGG	ENSP00000514856.2:n.8632+15_8632+18delinsATGG
ENST00000700202.1:c.1099+15_1099+18delinsATGG	ENSP00000514856.1:n.1099+15_1099+18delinsATGG
ENST00000380152.8:c.8632+15_8632+18delinsATGG MANE Select	ENSP00000369497.3:n.8632+15_8632+18delinsATGG
ENST00000544455.6:c.8632+15_8632+18delinsATGG	ENSP00000439902.1:n.8632+15_8632+18delinsATGG
ENST00000614259.2:c.8640+15_8640+18delinsATGG	ENSP00000506251.1:n.8640+15_8640+18delinsATGG
ENST00000665585.1:c.1197+15_1197+18delinsATGG
ENST00000680887.1:c.8632+15_8632+18delinsATGG	ENSP00000505508.1:n.8632+15_8632+18delinsATGG
ENST00000380152.7:c.8632+15_8632+18delinsATGG	ENSP00000369497.3:n.8632+15_8632+18delinsATGG
ENST00000528762.1:c.130+15_130+18delinsATGG	ENSP00000433168.1:n.130+15_130+18delinsATGG
ENST00000544455.5:c.8632+15_8632+18delinsATGG	ENSP00000439902.1:n.8632+15_8632+18delinsATGG
NM_000059.3:c.8632+15_8632+18delinsATGG , LRG_293t1:c.8632+15_8632+18delinsATGG	NP_000050.2:n.8632+15_8632+18delinsATGG
XM_011535203.1:c.8632+15_8632+18delinsATGG	XP_011533505.1:n.8632+15_8632+18delinsATGG
XM_011535204.1:c.8536+15_8536+18delinsATGG	XP_011533506.1:n.8536+15_8536+18delinsATGG
XM_011535205.1:c.8632+15_8632+18delinsATGG	XP_011533507.1:n.8632+15_8632+18delinsATGG
NM_000059.4:c.8632+15_8632+18delinsATGG MANE Select	NP_000050.3:n.8632+15_8632+18delinsATGG