Canonical Allele Identifier: CA387767607

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 3075159
• ClinVar RCV Id: RCV004015685
• dbSNP Id: rs1057520433
• MyVariant Identifiers: chr13:g.32972640A>T (hg19) ; chr13:g.32398503A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398503A>T , CM000675.2:g.32398503A>T	GRCh38
NC_000013.10:g.32972640A>T , CM000675.1:g.32972640A>T	GRCh37
NC_000013.9:g.31870640A>T	NCBI36
NG_012772.3:g.88024A>T , LRG_293:g.88024A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*513A>T	ENSP00000434898.2:n.*513A>T
ENST00000528762.2:c.*1357A>T	ENSP00000433168.2:n.*1357A>T
ENST00000530893.7:c.9621A>T	ENSP00000499438.2:p.Glu3207Asp
ENST00000665585.2:c.*1552A>T	ENSP00000499570.2:n.*1552A>T
ENST00000700202.2:c.9939A>T	ENSP00000514856.2:p.Glu3313Asp
ENST00000700202.1:c.2406A>T	ENSP00000514856.1:p.Glu802Asp
ENST00000700203.1:n.2117A>T
ENST00000380152.8:c.9990A>T MANE Select	ENSP00000369497.3:p.Glu3330Asp
ENST00000544455.6:c.9990A>T	ENSP00000439902.1:p.Glu3330Asp
ENST00000614259.2:c.9998A>T	ENSP00000506251.1:n.9998A>T
ENST00000680887.1:c.9990A>T	ENSP00000505508.1:p.Glu3330Asp
ENST00000380152.7:c.9990A>T	ENSP00000369497.3:p.Glu3330Asp
ENST00000544455.5:c.9990A>T	ENSP00000439902.1:p.Glu3330Asp
NM_000059.3:c.9990A>T , LRG_293t1:c.9990A>T	NP_000050.2:p.Glu3330Asp
XM_011535203.1:c.9990A>T	XP_011533505.1:p.Glu3330Asp
XM_011535204.1:c.9894A>T	XP_011533506.1:p.Glu3298Asp
NM_000059.4:c.9990A>T MANE Select	NP_000050.3:p.Glu3330Asp