Canonical Allele Identifier: CA2082814879

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32370743_32370745delinsGCC , CM000675.2:g.32370743_32370745delinsGCC	GRCh38
NC_000013.10:g.32944880_32944882delinsGCC , CM000675.1:g.32944880_32944882delinsGCC	GRCh37
NC_000013.9:g.31842880_31842882delinsGCC	NCBI36
NG_012772.3:g.60264_60266delinsGCC , LRG_293:g.60264_60266delinsGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8487+186_8487+188delinsGCC	ENSP00000434898.2:n.8487+186_8487+188delinsGCC
ENST00000528762.2:c.8487+186_8487+188delinsGCC	ENSP00000433168.2:n.8487+186_8487+188delinsGCC
ENST00000530893.7:c.8118+186_8118+188delinsGCC	ENSP00000499438.2:n.8118+186_8118+188delinsGCC
ENST00000665585.2:c.8487+186_8487+188delinsGCC	ENSP00000499570.2:n.8487+186_8487+188delinsGCC
ENST00000666593.2:c.8487+186_8487+188delinsGCC	ENSP00000499256.2:n.8487+186_8487+188delinsGCC
ENST00000700202.2:c.8487+186_8487+188delinsGCC	ENSP00000514856.2:n.8487+186_8487+188delinsGCC
ENST00000700202.1:c.954+186_954+188delinsGCC	ENSP00000514856.1:n.954+186_954+188delinsGCC
ENST00000380152.8:c.8487+186_8487+188delinsGCC MANE Select	ENSP00000369497.3:n.8487+186_8487+188delinsGCC
ENST00000544455.6:c.8487+186_8487+188delinsGCC	ENSP00000439902.1:n.8487+186_8487+188delinsGCC
ENST00000614259.2:c.8495+186_8495+188delinsGCC	ENSP00000506251.1:n.8495+186_8495+188delinsGCC
ENST00000665585.1:c.1052+186_1052+188delinsGCC
ENST00000680887.1:c.8487+186_8487+188delinsGCC	ENSP00000505508.1:n.8487+186_8487+188delinsGCC
ENST00000380152.7:c.8487+186_8487+188delinsGCC	ENSP00000369497.3:n.8487+186_8487+188delinsGCC
ENST00000544455.5:c.8487+186_8487+188delinsGCC	ENSP00000439902.1:n.8487+186_8487+188delinsGCC
NM_000059.3:c.8487+186_8487+188delinsGCC , LRG_293t1:c.8487+186_8487+188delinsGCC	NP_000050.2:n.8487+186_8487+188delinsGCC
XM_011535203.1:c.8487+186_8487+188delinsGCC	XP_011533505.1:n.8487+186_8487+188delinsGCC
XM_011535204.1:c.8391+186_8391+188delinsGCC	XP_011533506.1:n.8391+186_8391+188delinsGCC
XM_011535205.1:c.8487+186_8487+188delinsGCC	XP_011533507.1:n.8487+186_8487+188delinsGCC
NM_000059.4:c.8487+186_8487+188delinsGCC MANE Select	NP_000050.3:n.8487+186_8487+188delinsGCC