Canonical Allele Identifier: CA1139663180

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 918297
• ClinVar RCV Id: RCV001175803
• dbSNP Id: rs2072874502

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32376687del , CM000675.2:g.32376687del	GRCh38
NC_000013.10:g.32950824del , CM000675.1:g.32950824del	GRCh37
NC_000013.9:g.31848824del	NCBI36
NG_012772.3:g.66208del , LRG_293:g.66208del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8650del	ENSP00000434898.2:p.Tyr2884IlefsTer7
ENST00000528762.2:c.*17del	ENSP00000433168.2:n.*17del
ENST00000530893.7:c.8281del	ENSP00000499438.2:p.Tyr2761IlefsTer7
ENST00000665585.2:c.*212del	ENSP00000499570.2:n.*212del
ENST00000666593.2:c.8650del	ENSP00000499256.2:p.Tyr2884IlefsTer7
ENST00000700202.2:c.8650del	ENSP00000514856.2:p.Tyr2884IlefsTer7
ENST00000700202.1:c.1117del	ENSP00000514856.1:p.Tyr373IlefsTer7
ENST00000700203.1:n.777del
ENST00000380152.8:c.8650del MANE Select	ENSP00000369497.3:p.Tyr2884IlefsTer7
ENST00000544455.6:c.8650del	ENSP00000439902.1:p.Tyr2884IlefsTer7
ENST00000614259.2:c.8658del	ENSP00000506251.1:n.8658del
ENST00000665585.1:c.1528del
ENST00000680887.1:c.8650del	ENSP00000505508.1:p.Tyr2884IlefsTer7
ENST00000380152.7:c.8650del	ENSP00000369497.3:p.Tyr2884IlefsTer7
ENST00000528762.1:c.212del	ENSP00000433168.1:n.212del
ENST00000544455.5:c.8650del	ENSP00000439902.1:p.Tyr2884IlefsTer7
NM_000059.3:c.8650del , LRG_293t1:c.8650del	NP_000050.2:p.Tyr2884IlefsTer7
XM_011535203.1:c.8650del	XP_011533505.1:p.Tyr2884IlefsTer7
XM_011535204.1:c.8554del	XP_011533506.1:p.Tyr2852IlefsTer7
XM_011535205.1:c.8650del	XP_011533507.1:p.Tyr2884IlefsTer7
NM_000059.4:c.8650del MANE Select	NP_000050.3:p.Tyr2884IlefsTer7