Canonical Allele Identifier: CA011927

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 51119
• ClinVar RCV Id: RCV000043800 ; RCV000257191 ; RCV000774912 ; RCV001385857
• dbSNP Id: rs397507586
• MyVariant Identifiers: chr13:g.32907020_32907021del (hg19) ; chr13:g.32332883_32332884del (hg38)
• PubMed: PMID:11802209

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32332883_32332884del , CM000675.2:g.32332883_32332884del	GRCh38
NC_000013.10:g.32907020_32907021del , CM000675.1:g.32907020_32907021del	GRCh37
NC_000013.9:g.31805020_31805021del	NCBI36
NG_012772.3:g.22404_22405del , LRG_293:g.22404_22405del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.1405_1406del	ENSP00000434898.2:p.Asp469Ter
ENST00000528762.2:c.1405_1406del	ENSP00000433168.2:p.Asp469Ter
ENST00000530893.7:c.1036_1037del	ENSP00000499438.2:p.Asp346Ter
ENST00000665585.2:c.1405_1406del	ENSP00000499570.2:p.Asp469Ter
ENST00000666593.2:c.1405_1406del	ENSP00000499256.2:p.Asp469Ter
ENST00000700202.2:c.1405_1406del	ENSP00000514856.2:p.Asp469Ter
ENST00000700201.1:c.*1184_*1185del	ENSP00000514855.1:n.*1184_*1185del
ENST00000380152.8:c.1405_1406del MANE Select	ENSP00000369497.3:p.Asp469Ter
ENST00000544455.6:c.1405_1406del	ENSP00000439902.1:p.Asp469Ter
ENST00000614259.2:c.1405_1406del	ENSP00000506251.1:p.Asp469Ter
ENST00000680887.1:c.1405_1406del	ENSP00000505508.1:p.Asp469Ter
ENST00000380152.7:c.1405_1406del	ENSP00000369497.3:p.Asp469Ter
ENST00000530893.6:n.1603_1604del
ENST00000544455.5:c.1405_1406del	ENSP00000439902.1:p.Asp469Ter
ENST00000614259.1:n.1405_1406del
NM_000059.3:c.1405_1406del , LRG_293t1:c.1405_1406del	NP_000050.2:p.Asp469Ter
XM_011535203.1:c.1405_1406del	XP_011533505.1:p.Asp469Ter
XM_011535204.1:c.1405_1406del	XP_011533506.1:p.Asp469Ter
XM_011535205.1:c.1405_1406del	XP_011533507.1:p.Asp469Ter
NM_000059.4:c.1405_1406del MANE Select	NP_000050.3:p.Asp469Ter