Canonical Allele Identifier: CA2082835722

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32379376_32379380delinsTAAGA , CM000675.2:g.32379376_32379380delinsTAAGA	GRCh38
NC_000013.10:g.32953513_32953517delinsTAAGA , CM000675.1:g.32953513_32953517delinsTAAGA	GRCh37
NC_000013.9:g.31851513_31851517delinsTAAGA	NCBI36
NG_012772.3:g.68897_68901delinsTAAGA , LRG_293:g.68897_68901delinsTAAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8814_8818delinsTAAGA	ENSP00000434898.2:p.Asp2938=
ENST00000528762.2:c.*181_*185delinsTAAGA	ENSP00000433168.2:n.*181_*185delinsTAAGA
ENST00000530893.7:c.8445_8449delinsTAAGA	ENSP00000499438.2:p.Asp2815=
ENST00000665585.2:c.*376_*380delinsTAAGA	ENSP00000499570.2:n.*376_*380delinsTAAGA
ENST00000666593.2:c.8814_8818delinsTAAGA	ENSP00000499256.2:p.Asp2938=
ENST00000700202.2:c.8814_8818delinsTAAGA	ENSP00000514856.2:p.Asp2938=
ENST00000700202.1:c.1281_1285delinsTAAGA	ENSP00000514856.1:p.Asp427=
ENST00000700203.1:n.941_945delinsTAAGA
ENST00000380152.8:c.8814_8818delinsTAAGA MANE Select	ENSP00000369497.3:p.Asp2938=
ENST00000544455.6:c.8814_8818delinsTAAGA	ENSP00000439902.1:p.Asp2938=
ENST00000614259.2:c.8822_8826delinsTAAGA	ENSP00000506251.1:n.8822_8826delinsTAAGA
ENST00000665585.1:c.1692_1696delinsTAAGA
ENST00000680887.1:c.8814_8818delinsTAAGA	ENSP00000505508.1:p.Asp2938=
ENST00000380152.7:c.8814_8818delinsTAAGA	ENSP00000369497.3:p.Asp2938=
ENST00000528762.1:c.376_380delinsTAAGA	ENSP00000433168.1:n.376_380delinsTAAGA
ENST00000544455.5:c.8814_8818delinsTAAGA	ENSP00000439902.1:p.Asp2938=
NM_000059.3:c.8814_8818delinsTAAGA , LRG_293t1:c.8814_8818delinsTAAGA	NP_000050.2:p.Asp2938=
XM_011535203.1:c.8814_8818delinsTAAGA	XP_011533505.1:p.Asp2938=
XM_011535204.1:c.8718_8722delinsTAAGA	XP_011533506.1:p.Asp2906=
XM_011535205.1:c.8755-374_8755-370delinsTAAGA	XP_011533507.1:n.8755-374_8755-370delinsTAAGA
NM_000059.4:c.8814_8818delinsTAAGA MANE Select	NP_000050.3:p.Asp2938=