Canonical Allele Identifier: CA16613986

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 409557
• ClinVar RCV Id: RCV000468326 ; RCV003278815
• dbSNP Id: rs1060502464
• MyVariant Identifiers: chr13:g.32972592A>C (hg19) ; chr13:g.32398455A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398455A>C , CM000675.2:g.32398455A>C	GRCh38
NC_000013.10:g.32972592A>C , CM000675.1:g.32972592A>C	GRCh37
NC_000013.9:g.31870592A>C	NCBI36
NG_012772.3:g.87976A>C , LRG_293:g.87976A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*465A>C	ENSP00000434898.2:n.*465A>C
ENST00000528762.2:c.*1309A>C	ENSP00000433168.2:n.*1309A>C
ENST00000530893.7:c.9573A>C	ENSP00000499438.2:p.Lys3191Asn
ENST00000665585.2:c.*1504A>C	ENSP00000499570.2:n.*1504A>C
ENST00000700202.2:c.9891A>C	ENSP00000514856.2:p.Lys3297Asn
ENST00000700202.1:c.2358A>C	ENSP00000514856.1:p.Lys786Asn
ENST00000700203.1:n.2069A>C
ENST00000380152.8:c.9942A>C MANE Select	ENSP00000369497.3:p.Lys3314Asn
ENST00000544455.6:c.9942A>C	ENSP00000439902.1:p.Lys3314Asn
ENST00000614259.2:c.9950A>C	ENSP00000506251.1:n.9950A>C
ENST00000680887.1:c.9942A>C	ENSP00000505508.1:p.Lys3314Asn
ENST00000380152.7:c.9942A>C	ENSP00000369497.3:p.Lys3314Asn
ENST00000544455.5:c.9942A>C	ENSP00000439902.1:p.Lys3314Asn
NM_000059.3:c.9942A>C , LRG_293t1:c.9942A>C	NP_000050.2:p.Lys3314Asn
XM_011535203.1:c.9942A>C	XP_011533505.1:p.Lys3314Asn
XM_011535204.1:c.9846A>C	XP_011533506.1:p.Lys3282Asn
NM_000059.4:c.9942A>C MANE Select	NP_000050.3:p.Lys3314Asn