Canonical Allele Identifier: CA2082827232

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32376332_32376333delinsGC , CM000675.2:g.32376332_32376333delinsGC	GRCh38
NC_000013.10:g.32950469_32950470delinsGC , CM000675.1:g.32950469_32950470delinsGC	GRCh37
NC_000013.9:g.31848469_31848470delinsGC	NCBI36
NG_012772.3:g.65853_65854delinsGC , LRG_293:g.65853_65854delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8633-338_8633-337delinsGC	ENSP00000434898.2:n.8633-338_8633-337delinsGC
ENST00000528762.2:c.8697-338_8697-337delinsGC	ENSP00000433168.2:n.8697-338_8697-337delinsGC
ENST00000530893.7:c.8264-338_8264-337delinsGC	ENSP00000499438.2:n.8264-338_8264-337delinsGC
ENST00000665585.2:c.*195-338_*195-337delinsGC	ENSP00000499570.2:n.*195-338_*195-337delinsGC
ENST00000666593.2:c.8633-338_8633-337delinsGC	ENSP00000499256.2:n.8633-338_8633-337delinsGC
ENST00000700202.2:c.8633-338_8633-337delinsGC	ENSP00000514856.2:n.8633-338_8633-337delinsGC
ENST00000700202.1:c.1100-338_1100-337delinsGC	ENSP00000514856.1:n.1100-338_1100-337delinsGC
ENST00000700203.1:n.422_423delinsGC
ENST00000380152.8:c.8633-338_8633-337delinsGC MANE Select	ENSP00000369497.3:n.8633-338_8633-337delinsGC
ENST00000544455.6:c.8633-338_8633-337delinsGC	ENSP00000439902.1:n.8633-338_8633-337delinsGC
ENST00000614259.2:c.8641-338_8641-337delinsGC	ENSP00000506251.1:n.8641-338_8641-337delinsGC
ENST00000665585.1:c.1511-338_1511-337delinsGC
ENST00000680887.1:c.8633-338_8633-337delinsGC	ENSP00000505508.1:n.8633-338_8633-337delinsGC
ENST00000380152.7:c.8633-338_8633-337delinsGC	ENSP00000369497.3:n.8633-338_8633-337delinsGC
ENST00000528762.1:c.195-338_195-337delinsGC	ENSP00000433168.1:n.195-338_195-337delinsGC
ENST00000544455.5:c.8633-338_8633-337delinsGC	ENSP00000439902.1:n.8633-338_8633-337delinsGC
NM_000059.3:c.8633-338_8633-337delinsGC , LRG_293t1:c.8633-338_8633-337delinsGC	NP_000050.2:n.8633-338_8633-337delinsGC
XM_011535203.1:c.8633-338_8633-337delinsGC	XP_011533505.1:n.8633-338_8633-337delinsGC
XM_011535204.1:c.8537-338_8537-337delinsGC	XP_011533506.1:n.8537-338_8537-337delinsGC
XM_011535205.1:c.8633-338_8633-337delinsGC	XP_011533507.1:n.8633-338_8633-337delinsGC
NM_000059.4:c.8633-338_8633-337delinsGC MANE Select	NP_000050.3:n.8633-338_8633-337delinsGC