Canonical Allele Identifier: CA658823560

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 548352
• ClinVar RCV Id: RCV000661502
• dbSNP Id: rs80359419
• MyVariant Identifiers: chr13:g.32912498_32912499insCATC (hg19) ; chr13:g.32338361_32338362insCATC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32338361_32338362insCATC , CM000675.2:g.32338361_32338362insCATC	GRCh38
NC_000013.10:g.32912498_32912499insCATC , CM000675.1:g.32912498_32912499insCATC	GRCh37
NC_000013.9:g.31810498_31810499insCATC	NCBI36
NG_012772.3:g.27882_27883insCATC , LRG_293:g.27882_27883insCATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.4006_4007insCATC	ENSP00000434898.2:p.Phe1336SerfsTer3
ENST00000528762.2:c.4006_4007insCATC	ENSP00000433168.2:p.Phe1336SerfsTer3
ENST00000530893.7:c.3637_3638insCATC	ENSP00000499438.2:p.Phe1213SerfsTer3
ENST00000665585.2:c.4006_4007insCATC	ENSP00000499570.2:p.Phe1336SerfsTer3
ENST00000666593.2:c.4006_4007insCATC	ENSP00000499256.2:p.Phe1336SerfsTer3
ENST00000700202.2:c.4006_4007insCATC	ENSP00000514856.2:p.Phe1336SerfsTer3
ENST00000380152.8:c.4006_4007insCATC MANE Select	ENSP00000369497.3:p.Phe1336SerfsTer3
ENST00000544455.6:c.4006_4007insCATC	ENSP00000439902.1:p.Phe1336SerfsTer3
ENST00000614259.2:c.4006_4007insCATC	ENSP00000506251.1:p.Phe1336SerfsTer3
ENST00000680887.1:c.4006_4007insCATC	ENSP00000505508.1:p.Phe1336SerfsTer3
ENST00000380152.7:c.4006_4007insCATC	ENSP00000369497.3:p.Phe1336SerfsTer3
ENST00000544455.5:c.4006_4007insCATC	ENSP00000439902.1:p.Phe1336SerfsTer3
ENST00000614259.1:n.4006_4007insCATC
NM_000059.3:c.4006_4007insCATC , LRG_293t1:c.4006_4007insCATC	NP_000050.2:p.Phe1336SerfsTer3
XM_011535203.1:c.4006_4007insCATC	XP_011533505.1:p.Phe1336SerfsTer3
XM_011535204.1:c.4006_4007insCATC	XP_011533506.1:p.Phe1336SerfsTer3
XM_011535205.1:c.4006_4007insCATC	XP_011533507.1:p.Phe1336SerfsTer3
NM_000059.4:c.4006_4007insCATC MANE Select	NP_000050.3:p.Phe1336SerfsTer3