Canonical Allele Identifier: CA2082831829

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32362650_32362651delinsAG , CM000675.2:g.32362650_32362651delinsAG	GRCh38
NC_000013.10:g.32936787_32936788delinsAG , CM000675.1:g.32936787_32936788delinsAG	GRCh37
NC_000013.9:g.31834787_31834788delinsAG	NCBI36
NG_012772.3:g.52171_52172delinsAG , LRG_293:g.52171_52172delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7933_7934delinsAG	ENSP00000434898.2:p.Arg2645=
ENST00000528762.2:c.7933_7934delinsAG	ENSP00000433168.2:p.Arg2645=
ENST00000530893.7:c.7564_7565delinsAG	ENSP00000499438.2:p.Arg2522=
ENST00000665585.2:c.7933_7934delinsAG	ENSP00000499570.2:p.Arg2645=
ENST00000666593.2:c.7933_7934delinsAG	ENSP00000499256.2:p.Arg2645=
ENST00000700202.2:c.7933_7934delinsAG	ENSP00000514856.2:p.Arg2645=
ENST00000700202.1:c.400_401delinsAG	ENSP00000514856.1:p.Arg134=
ENST00000380152.8:c.7933_7934delinsAG MANE Select	ENSP00000369497.3:p.Arg2645=
ENST00000544455.6:c.7933_7934delinsAG	ENSP00000439902.1:p.Arg2645=
ENST00000614259.2:c.7941_7942delinsAG	ENSP00000506251.1:p.Ile2647=
ENST00000665585.1:c.498_499delinsAG
ENST00000680887.1:c.7933_7934delinsAG	ENSP00000505508.1:p.Arg2645=
ENST00000380152.7:c.7933_7934delinsAG	ENSP00000369497.3:p.Arg2645=
ENST00000544455.5:c.7933_7934delinsAG	ENSP00000439902.1:p.Arg2645=
ENST00000614259.1:n.7941_7942delinsAG
NM_000059.3:c.7933_7934delinsAG , LRG_293t1:c.7933_7934delinsAG	NP_000050.2:p.Arg2645=
XM_011535203.1:c.7933_7934delinsAG	XP_011533505.1:p.Arg2645=
XM_011535204.1:c.7837_7838delinsAG	XP_011533506.1:p.Arg2613=
XM_011535205.1:c.7933_7934delinsAG	XP_011533507.1:p.Arg2645=
NM_000059.4:c.7933_7934delinsAG MANE Select	NP_000050.3:p.Arg2645=