Canonical Allele Identifier: CA2580614696

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 2431322
• ClinVar RCV Id: RCV003140382

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32340226_32340227del , CM000675.2:g.32340226_32340227del	GRCh38
NC_000013.10:g.32914363_32914364del , CM000675.1:g.32914363_32914364del	GRCh37
NC_000013.9:g.31812363_31812364del	NCBI36
NG_012772.3:g.29747_29748del , LRG_293:g.29747_29748del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.5871_5872del	ENSP00000434898.2:p.Ile1957MetfsTer2
ENST00000528762.2:c.5871_5872del	ENSP00000433168.2:p.Ile1957MetfsTer2
ENST00000530893.7:c.5502_5503del	ENSP00000499438.2:p.Ile1834MetfsTer2
ENST00000665585.2:c.5871_5872del	ENSP00000499570.2:p.Ile1957MetfsTer2
ENST00000666593.2:c.5871_5872del	ENSP00000499256.2:p.Ile1957MetfsTer2
ENST00000700202.2:c.5871_5872del	ENSP00000514856.2:p.Ile1957MetfsTer2
ENST00000380152.8:c.5871_5872del MANE Select	ENSP00000369497.3:p.Ile1957MetfsTer2
ENST00000544455.6:c.5871_5872del	ENSP00000439902.1:p.Ile1957MetfsTer2
ENST00000614259.2:c.5871_5872del	ENSP00000506251.1:p.Ile1957MetfsTer2
ENST00000680887.1:c.5871_5872del	ENSP00000505508.1:p.Ile1957MetfsTer2
ENST00000380152.7:c.5871_5872del	ENSP00000369497.3:p.Ile1957MetfsTer2
ENST00000544455.5:c.5871_5872del	ENSP00000439902.1:p.Ile1957MetfsTer2
ENST00000614259.1:n.5871_5872del
NM_000059.3:c.5871_5872del , LRG_293t1:c.5871_5872del	NP_000050.2:p.Ile1957MetfsTer2
XM_011535203.1:c.5871_5872del	XP_011533505.1:p.Ile1957MetfsTer2
XM_011535204.1:c.5871_5872del	XP_011533506.1:p.Ile1957MetfsTer2
XM_011535205.1:c.5871_5872del	XP_011533507.1:p.Ile1957MetfsTer2
NM_000059.4:c.5871_5872del MANE Select	NP_000050.3:p.Ile1957MetfsTer2