Canonical Allele Identifier: CA2082836999

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32379595_32379602delinsGATAAAGT , CM000675.2:g.32379595_32379602delinsGATAAAGT	GRCh38
NC_000013.10:g.32953732_32953739delinsGATAAAGT , CM000675.1:g.32953732_32953739delinsGATAAAGT	GRCh37
NC_000013.9:g.31851732_31851739delinsGATAAAGT	NCBI36
NG_012772.3:g.69116_69123delinsGATAAAGT , LRG_293:g.69116_69123delinsGATAAAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8953+80_8953+87delinsGATAAAGT	ENSP00000434898.2:n.8953+80_8953+87delinsGATAAAGT
ENST00000528762.2:c.*320+80_*320+87delinsGATAAAGT	ENSP00000433168.2:n.*320+80_*320+87delinsGATAAAGT
ENST00000530893.7:c.8584+80_8584+87delinsGATAAAGT	ENSP00000499438.2:n.8584+80_8584+87delinsGATAAAGT
ENST00000665585.2:c.*515+80_*515+87delinsGATAAAGT	ENSP00000499570.2:n.*515+80_*515+87delinsGATAAAGT
ENST00000666593.2:c.8953+80_8953+87delinsGATAAAGT	ENSP00000499256.2:n.8953+80_8953+87delinsGATAAAGT
ENST00000700202.2:c.8953+80_8953+87delinsGATAAAGT	ENSP00000514856.2:n.8953+80_8953+87delinsGATAAAGT
ENST00000700202.1:c.1420+80_1420+87delinsGATAAAGT	ENSP00000514856.1:n.1420+80_1420+87delinsGATAAAGT
ENST00000700203.1:n.1080+80_1080+87delinsGATAAAGT
ENST00000380152.8:c.8953+80_8953+87delinsGATAAAGT MANE Select	ENSP00000369497.3:n.8953+80_8953+87delinsGATAAAGT
ENST00000544455.6:c.8953+80_8953+87delinsGATAAAGT	ENSP00000439902.1:n.8953+80_8953+87delinsGATAAAGT
ENST00000614259.2:c.8961+80_8961+87delinsGATAAAGT	ENSP00000506251.1:n.8961+80_8961+87delinsGATAAAGT
ENST00000665585.1:c.1831+80_1831+87delinsGATAAAGT
ENST00000680887.1:c.8953+80_8953+87delinsGATAAAGT	ENSP00000505508.1:n.8953+80_8953+87delinsGATAAAGT
ENST00000380152.7:c.8953+80_8953+87delinsGATAAAGT	ENSP00000369497.3:n.8953+80_8953+87delinsGATAAAGT
ENST00000544455.5:c.8953+80_8953+87delinsGATAAAGT	ENSP00000439902.1:n.8953+80_8953+87delinsGATAAAGT
NM_000059.3:c.8953+80_8953+87delinsGATAAAGT , LRG_293t1:c.8953+80_8953+87delinsGATAAAGT	NP_000050.2:n.8953+80_8953+87delinsGATAAAGT
XM_011535203.1:c.8953+80_8953+87delinsGATAAAGT	XP_011533505.1:n.8953+80_8953+87delinsGATAAAGT
XM_011535204.1:c.8857+80_8857+87delinsGATAAAGT	XP_011533506.1:n.8857+80_8857+87delinsGATAAAGT
XM_011535205.1:c.8755-155_8755-148delinsGATAAAGT	XP_011533507.1:n.8755-155_8755-148delinsGATAAAGT
NM_000059.4:c.8953+80_8953+87delinsGATAAAGT MANE Select	NP_000050.3:n.8953+80_8953+87delinsGATAAAGT