Canonical Allele Identifier: CA2082754648

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32328029_32328030delinsCA , CM000675.2:g.32328029_32328030delinsCA	GRCh38
NC_000013.10:g.32902166_32902167delinsCA , CM000675.1:g.32902166_32902167delinsCA	GRCh37
NC_000013.9:g.31800166_31800167delinsCA	NCBI36
NG_012772.3:g.17550_17551delinsCA , LRG_293:g.17550_17551delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.632-1414_632-1413delinsCA	ENSP00000434898.2:n.632-1414_632-1413delinsCA
ENST00000528762.2:c.632-1414_632-1413delinsCA	ENSP00000433168.2:n.632-1414_632-1413delinsCA
ENST00000530893.7:c.263-1414_263-1413delinsCA	ENSP00000499438.2:n.263-1414_263-1413delinsCA
ENST00000665585.2:c.632-1414_632-1413delinsCA	ENSP00000499570.2:n.632-1414_632-1413delinsCA
ENST00000666593.2:c.632-1414_632-1413delinsCA	ENSP00000499256.2:n.632-1414_632-1413delinsCA
ENST00000700202.2:c.632-1414_632-1413delinsCA	ENSP00000514856.2:n.632-1414_632-1413delinsCA
ENST00000700201.1:c.*411-1414_*411-1413delinsCA	ENSP00000514855.1:n.*411-1414_*411-1413delinsCA
ENST00000380152.8:c.632-1414_632-1413delinsCA MANE Select	ENSP00000369497.3:n.632-1414_632-1413delinsCA
ENST00000544455.6:c.632-1414_632-1413delinsCA	ENSP00000439902.1:n.632-1414_632-1413delinsCA
ENST00000614259.2:c.632-1414_632-1413delinsCA	ENSP00000506251.1:n.632-1414_632-1413delinsCA
ENST00000680887.1:c.632-1414_632-1413delinsCA	ENSP00000505508.1:n.632-1414_632-1413delinsCA
ENST00000380152.7:c.632-1414_632-1413delinsCA	ENSP00000369497.3:n.632-1414_632-1413delinsCA
ENST00000530893.6:n.830-1414_830-1413delinsCA
ENST00000544455.5:c.632-1414_632-1413delinsCA	ENSP00000439902.1:n.632-1414_632-1413delinsCA
ENST00000614259.1:n.632-1414_632-1413delinsCA
NM_000059.3:c.632-1414_632-1413delinsCA , LRG_293t1:c.632-1414_632-1413delinsCA	NP_000050.2:n.632-1414_632-1413delinsCA
XM_011535203.1:c.632-1414_632-1413delinsCA	XP_011533505.1:n.632-1414_632-1413delinsCA
XM_011535204.1:c.632-1414_632-1413delinsCA	XP_011533506.1:n.632-1414_632-1413delinsCA
XM_011535205.1:c.632-1414_632-1413delinsCA	XP_011533507.1:n.632-1414_632-1413delinsCA
NM_000059.4:c.632-1414_632-1413delinsCA MANE Select	NP_000050.3:n.632-1414_632-1413delinsCA