Canonical Allele Identifier: CA2573149394

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 1416629
• ClinVar RCV Id: RCV001923401
• dbSNP Id: rs2137563070

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32356555del , CM000675.2:g.32356555del	GRCh38
NC_000013.10:g.32930692del , CM000675.1:g.32930692del	GRCh37
NC_000013.9:g.31828692del	NCBI36
NG_012772.3:g.46076del , LRG_293:g.46076del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7563del	ENSP00000434898.2:p.Ser2522LeufsTer2
ENST00000528762.2:c.7563del	ENSP00000433168.2:p.Ser2522LeufsTer2
ENST00000530893.7:c.7194del	ENSP00000499438.2:p.Ser2399LeufsTer2
ENST00000665585.2:c.7563del	ENSP00000499570.2:p.Ser2522LeufsTer2
ENST00000666593.2:c.7563del	ENSP00000499256.2:p.Ser2522LeufsTer2
ENST00000700202.2:c.7563del	ENSP00000514856.2:p.Ser2522LeufsTer2
ENST00000700202.1:c.30del	ENSP00000514856.1:p.Ser11LeufsTer2
ENST00000380152.8:c.7563del MANE Select	ENSP00000369497.3:p.Ser2522LeufsTer2
ENST00000544455.6:c.7563del	ENSP00000439902.1:p.Ser2522LeufsTer2
ENST00000614259.2:c.7563del	ENSP00000506251.1:p.Ser2522LeufsTer2
ENST00000665585.1:c.128del
ENST00000680887.1:c.7563del	ENSP00000505508.1:p.Ser2522LeufsTer2
ENST00000380152.7:c.7563del	ENSP00000369497.3:p.Ser2522LeufsTer2
ENST00000544455.5:c.7563del	ENSP00000439902.1:p.Ser2522LeufsTer2
ENST00000614259.1:n.7563del
NM_000059.3:c.7563del , LRG_293t1:c.7563del	NP_000050.2:p.Ser2522LeufsTer2
XM_011535203.1:c.7563del	XP_011533505.1:p.Ser2522LeufsTer2
XM_011535204.1:c.7467del	XP_011533506.1:p.Ser2490LeufsTer2
XM_011535205.1:c.7563del	XP_011533507.1:p.Ser2522LeufsTer2
NM_000059.4:c.7563del MANE Select	NP_000050.3:p.Ser2522LeufsTer2