Canonical Allele Identifier: CA2082812288

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32337236_32337261delinsCAGCATATAAAAATGACTCTAGGTCA , CM000675.2:g.32337236_32337261delinsCAGCATATAAAAATGACTCTAGGTCA	GRCh38
NC_000013.10:g.32911373_32911398delinsCAGCATATAAAAATGACTCTAGGTCA , CM000675.1:g.32911373_32911398delinsCAGCATATAAAAATGACTCTAGGTCA	GRCh37
NC_000013.9:g.31809373_31809398delinsCAGCATATAAAAATGACTCTAGGTCA	NCBI36
NG_012772.3:g.26757_26782delinsCAGCATATAAAAATGACTCTAGGTCA , LRG_293:g.26757_26782delinsCAGCATATAAAAATGACTCTAGGTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.2881_2906delinsCAGCATATAAAAATGACTCTAGGTCA	ENSP00000434898.2:p.Gln961=
ENST00000528762.2:c.2881_2906delinsCAGCATATAAAAATGACTCTAGGTCA	ENSP00000433168.2:p.Gln961=
ENST00000530893.7:c.2512_2537delinsCAGCATATAAAAATGACTCTAGGTCA	ENSP00000499438.2:p.Gln838=
ENST00000665585.2:c.2881_2906delinsCAGCATATAAAAATGACTCTAGGTCA	ENSP00000499570.2:p.Gln961=
ENST00000666593.2:c.2881_2906delinsCAGCATATAAAAATGACTCTAGGTCA	ENSP00000499256.2:p.Gln961=
ENST00000700202.2:c.2881_2906delinsCAGCATATAAAAATGACTCTAGGTCA	ENSP00000514856.2:p.Gln961=
ENST00000380152.8:c.2881_2906delinsCAGCATATAAAAATGACTCTAGGTCA MANE Select	ENSP00000369497.3:p.Gln961=
ENST00000544455.6:c.2881_2906delinsCAGCATATAAAAATGACTCTAGGTCA	ENSP00000439902.1:p.Gln961=
ENST00000614259.2:c.2881_2906delinsCAGCATATAAAAATGACTCTAGGTCA	ENSP00000506251.1:p.Gln961=
ENST00000680887.1:c.2881_2906delinsCAGCATATAAAAATGACTCTAGGTCA	ENSP00000505508.1:p.Gln961=
ENST00000380152.7:c.2881_2906delinsCAGCATATAAAAATGACTCTAGGTCA	ENSP00000369497.3:p.Gln961=
ENST00000544455.5:c.2881_2906delinsCAGCATATAAAAATGACTCTAGGTCA	ENSP00000439902.1:p.Gln961=
ENST00000614259.1:n.2881_2906delinsCAGCATATAAAAATGACTCTAGGTCA
NM_000059.3:c.2881_2906delinsCAGCATATAAAAATGACTCTAGGTCA , LRG_293t1:c.2881_2906delinsCAGCATATAAAAATGACTCTAGGTCA	NP_000050.2:p.Gln961=
XM_011535203.1:c.2881_2906delinsCAGCATATAAAAATGACTCTAGGTCA	XP_011533505.1:p.Gln961=
XM_011535204.1:c.2881_2906delinsCAGCATATAAAAATGACTCTAGGTCA	XP_011533506.1:p.Gln961=
XM_011535205.1:c.2881_2906delinsCAGCATATAAAAATGACTCTAGGTCA	XP_011533507.1:p.Gln961=
NM_000059.4:c.2881_2906delinsCAGCATATAAAAATGACTCTAGGTCA MANE Select	NP_000050.3:p.Gln961=