Canonical Allele Identifier: CA2082756522

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32329446_32329447delinsGA , CM000675.2:g.32329446_32329447delinsGA	GRCh38
NC_000013.10:g.32903583_32903584delinsGA , CM000675.1:g.32903583_32903584delinsGA	GRCh37
NC_000013.9:g.31801583_31801584delinsGA	NCBI36
NG_012772.3:g.18967_18968delinsGA , LRG_293:g.18967_18968delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.635_636delinsGA	ENSP00000434898.2:p.Arg212=
ENST00000528762.2:c.635_636delinsGA	ENSP00000433168.2:p.Arg212=
ENST00000530893.7:c.266_267delinsGA	ENSP00000499438.2:p.Arg89=
ENST00000665585.2:c.635_636delinsGA	ENSP00000499570.2:p.Arg212=
ENST00000666593.2:c.635_636delinsGA	ENSP00000499256.2:p.Arg212=
ENST00000700202.2:c.635_636delinsGA	ENSP00000514856.2:p.Arg212=
ENST00000700201.1:c.*414_*415delinsGA	ENSP00000514855.1:n.*414_*415delinsGA
ENST00000380152.8:c.635_636delinsGA MANE Select	ENSP00000369497.3:p.Arg212=
ENST00000544455.6:c.635_636delinsGA	ENSP00000439902.1:p.Arg212=
ENST00000614259.2:c.635_636delinsGA	ENSP00000506251.1:p.Arg212=
ENST00000680887.1:c.635_636delinsGA	ENSP00000505508.1:p.Arg212=
ENST00000380152.7:c.635_636delinsGA	ENSP00000369497.3:p.Arg212=
ENST00000530893.6:n.833_834delinsGA
ENST00000544455.5:c.635_636delinsGA	ENSP00000439902.1:p.Arg212=
ENST00000614259.1:n.635_636delinsGA
NM_000059.3:c.635_636delinsGA , LRG_293t1:c.635_636delinsGA	NP_000050.2:p.Arg212=
XM_011535203.1:c.635_636delinsGA	XP_011533505.1:p.Arg212=
XM_011535204.1:c.635_636delinsGA	XP_011533506.1:p.Arg212=
XM_011535205.1:c.635_636delinsGA	XP_011533507.1:p.Arg212=
NM_000059.4:c.635_636delinsGA MANE Select	NP_000050.3:p.Arg212=