Canonical Allele Identifier: CA2082832689

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32362788_32362801delinsCCAGTTGTCAGTGA , CM000675.2:g.32362788_32362801delinsCCAGTTGTCAGTGA	GRCh38
NC_000013.10:g.32936925_32936938delinsCCAGTTGTCAGTGA , CM000675.1:g.32936925_32936938delinsCCAGTTGTCAGTGA	GRCh37
NC_000013.9:g.31834925_31834938delinsCCAGTTGTCAGTGA	NCBI36
NG_012772.3:g.52309_52322delinsCCAGTTGTCAGTGA , LRG_293:g.52309_52322delinsCCAGTTGTCAGTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7976+95_7976+108delinsCCAGTTGTCAGTGA	ENSP00000434898.2:n.7976+95_7976+108delinsCCAGTTGTCAGTGA
ENST00000528762.2:c.7976+95_7976+108delinsCCAGTTGTCAGTGA	ENSP00000433168.2:n.7976+95_7976+108delinsCCAGTTGTCAGTGA
ENST00000530893.7:c.7607+95_7607+108delinsCCAGTTGTCAGTGA	ENSP00000499438.2:n.7607+95_7607+108delinsCCAGTTGTCAGTGA
ENST00000665585.2:c.7976+95_7976+108delinsCCAGTTGTCAGTGA	ENSP00000499570.2:n.7976+95_7976+108delinsCCAGTTGTCAGTGA
ENST00000666593.2:c.7976+95_7976+108delinsCCAGTTGTCAGTGA	ENSP00000499256.2:n.7976+95_7976+108delinsCCAGTTGTCAGTGA
ENST00000700202.2:c.7976+95_7976+108delinsCCAGTTGTCAGTGA	ENSP00000514856.2:n.7976+95_7976+108delinsCCAGTTGTCAGTGA
ENST00000700202.1:c.443+95_443+108delinsCCAGTTGTCAGTGA	ENSP00000514856.1:n.443+95_443+108delinsCCAGTTGTCAGTGA
ENST00000380152.8:c.7976+95_7976+108delinsCCAGTTGTCAGTGA MANE Select	ENSP00000369497.3:n.7976+95_7976+108delinsCCAGTTGTCAGTGA
ENST00000544455.6:c.7976+95_7976+108delinsCCAGTTGTCAGTGA	ENSP00000439902.1:n.7976+95_7976+108delinsCCAGTTGTCAGTGA
ENST00000614259.2:c.7984+95_7984+108delinsCCAGTTGTCAGTGA	ENSP00000506251.1:n.7984+95_7984+108delinsCCAGTTGTCAGTGA
ENST00000665585.1:c.541+95_541+108delinsCCAGTTGTCAGTGA
ENST00000680887.1:c.7976+95_7976+108delinsCCAGTTGTCAGTGA	ENSP00000505508.1:n.7976+95_7976+108delinsCCAGTTGTCAGTGA
ENST00000380152.7:c.7976+95_7976+108delinsCCAGTTGTCAGTGA	ENSP00000369497.3:n.7976+95_7976+108delinsCCAGTTGTCAGTGA
ENST00000544455.5:c.7976+95_7976+108delinsCCAGTTGTCAGTGA	ENSP00000439902.1:n.7976+95_7976+108delinsCCAGTTGTCAGTGA
NM_000059.3:c.7976+95_7976+108delinsCCAGTTGTCAGTGA , LRG_293t1:c.7976+95_7976+108delinsCCAGTTGTCAGTGA	NP_000050.2:n.7976+95_7976+108delinsCCAGTTGTCAGTGA
XM_011535203.1:c.7976+95_7976+108delinsCCAGTTGTCAGTGA	XP_011533505.1:n.7976+95_7976+108delinsCCAGTTGTCAGTGA
XM_011535204.1:c.7880+95_7880+108delinsCCAGTTGTCAGTGA	XP_011533506.1:n.7880+95_7880+108delinsCCAGTTGTCAGTGA
XM_011535205.1:c.7976+95_7976+108delinsCCAGTTGTCAGTGA	XP_011533507.1:n.7976+95_7976+108delinsCCAGTTGTCAGTGA
NM_000059.4:c.7976+95_7976+108delinsCCAGTTGTCAGTGA MANE Select	NP_000050.3:n.7976+95_7976+108delinsCCAGTTGTCAGTGA