Canonical Allele Identifier: CA2582341843

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 2583806
• ClinVar RCV Id: RCV003334728

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32337257_32337266del , CM000675.2:g.32337257_32337266del	GRCh38
NC_000013.10:g.32911394_32911403del , CM000675.1:g.32911394_32911403del	GRCh37
NC_000013.9:g.31809394_31809403del	NCBI36
NG_012772.3:g.26778_26787del , LRG_293:g.26778_26787del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.2902_2911del	ENSP00000434898.2:p.Gly968Ter
ENST00000528762.2:c.2902_2911del	ENSP00000433168.2:p.Gly968Ter
ENST00000530893.7:c.2533_2542del	ENSP00000499438.2:p.Gly845Ter
ENST00000665585.2:c.2902_2911del	ENSP00000499570.2:p.Gly968Ter
ENST00000666593.2:c.2902_2911del	ENSP00000499256.2:p.Gly968Ter
ENST00000700202.2:c.2902_2911del	ENSP00000514856.2:p.Gly968Ter
ENST00000380152.8:c.2902_2911del MANE Select	ENSP00000369497.3:p.Gly968Ter
ENST00000544455.6:c.2902_2911del	ENSP00000439902.1:p.Gly968Ter
ENST00000614259.2:c.2902_2911del	ENSP00000506251.1:p.Gly968Ter
ENST00000680887.1:c.2902_2911del	ENSP00000505508.1:p.Gly968Ter
ENST00000380152.7:c.2902_2911del	ENSP00000369497.3:p.Gly968Ter
ENST00000544455.5:c.2902_2911del	ENSP00000439902.1:p.Gly968Ter
ENST00000614259.1:n.2902_2911del
NM_000059.3:c.2902_2911del , LRG_293t1:c.2902_2911del	NP_000050.2:p.Gly968Ter
XM_011535203.1:c.2902_2911del	XP_011533505.1:p.Gly968Ter
XM_011535204.1:c.2902_2911del	XP_011533506.1:p.Gly968Ter
XM_011535205.1:c.2902_2911del	XP_011533507.1:p.Gly968Ter
NM_000059.4:c.2902_2911del MANE Select	NP_000050.3:p.Gly968Ter