Canonical Allele Identifier: CA2082780856

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32318439_32318441delinsATT , CM000675.2:g.32318439_32318441delinsATT	GRCh38
NC_000013.10:g.32892576_32892578delinsATT , CM000675.1:g.32892576_32892578delinsATT	GRCh37
NC_000013.9:g.31790576_31790578delinsATT	NCBI36
NG_012772.3:g.7960_7962delinsATT , LRG_293:g.7960_7962delinsATT
NG_017006.2:g.1923_1925delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.68-638_68-636delinsATT	ENSP00000434898.2:n.68-638_68-636delinsATT
ENST00000528762.2:c.68-638_68-636delinsATT	ENSP00000433168.2:n.68-638_68-636delinsATT
ENST00000530893.7:c.-302-638_-302-636delinsATT	ENSP00000499438.2:n.-302-638_-302-636delinsATT
ENST00000665585.2:c.68-638_68-636delinsATT	ENSP00000499570.2:n.68-638_68-636delinsATT
ENST00000666593.2:c.68-638_68-636delinsATT	ENSP00000499256.2:n.68-638_68-636delinsATT
ENST00000700202.2:c.68-638_68-636delinsATT	ENSP00000514856.2:n.68-638_68-636delinsATT
ENST00000700200.1:n.191+1912_191+1914delinsATT
ENST00000700201.1:c.68-638_68-636delinsATT	ENSP00000514855.1:n.68-638_68-636delinsATT
ENST00000380152.8:c.68-638_68-636delinsATT MANE Select	ENSP00000369497.3:n.68-638_68-636delinsATT
ENST00000544455.6:c.68-638_68-636delinsATT	ENSP00000439902.1:n.68-638_68-636delinsATT
ENST00000614259.2:c.68-638_68-636delinsATT	ENSP00000506251.1:n.68-638_68-636delinsATT
ENST00000680887.1:c.68-638_68-636delinsATT	ENSP00000505508.1:n.68-638_68-636delinsATT
ENST00000380152.7:c.68-638_68-636delinsATT	ENSP00000369497.3:n.68-638_68-636delinsATT
ENST00000530893.6:n.266-638_266-636delinsATT
ENST00000544455.5:c.68-638_68-636delinsATT	ENSP00000439902.1:n.68-638_68-636delinsATT
ENST00000614259.1:n.68-638_68-636delinsATT
NM_000059.3:c.68-638_68-636delinsATT , LRG_293t1:c.68-638_68-636delinsATT	NP_000050.2:n.68-638_68-636delinsATT
XM_011535203.1:c.68-638_68-636delinsATT	XP_011533505.1:n.68-638_68-636delinsATT
XM_011535204.1:c.68-638_68-636delinsATT	XP_011533506.1:n.68-638_68-636delinsATT
XM_011535205.1:c.68-638_68-636delinsATT	XP_011533507.1:n.68-638_68-636delinsATT
NM_000059.4:c.68-638_68-636delinsATT MANE Select	NP_000050.3:n.68-638_68-636delinsATT