Canonical Allele Identifier: CA387768581

Gene: BRCA2

Linked Data

• MyVariant Identifiers: chr13:g.32972880C>G (hg19) ; chr13:g.32398743C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398743C>G , CM000675.2:g.32398743C>G	GRCh38
NC_000013.10:g.32972880C>G , CM000675.1:g.32972880C>G	GRCh37
NC_000013.9:g.31870880C>G	NCBI36
NG_012772.3:g.88264C>G , LRG_293:g.88264C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*753C>G	ENSP00000434898.2:n.*753C>G
ENST00000528762.2:c.*1597C>G	ENSP00000433168.2:n.*1597C>G
ENST00000530893.7:c.9861C>G	ENSP00000499438.2:p.Asp3287Glu
ENST00000665585.2:c.*1792C>G	ENSP00000499570.2:n.*1792C>G
ENST00000700202.2:c.10179C>G	ENSP00000514856.2:p.Asp3393Glu
ENST00000700202.1:c.2646C>G	ENSP00000514856.1:p.Asp882Glu
ENST00000700203.1:n.2357C>G
ENST00000380152.8:c.10230C>G MANE Select	ENSP00000369497.3:p.Asp3410Glu
ENST00000544455.6:c.10230C>G	ENSP00000439902.1:p.Asp3410Glu
ENST00000614259.2:c.10238C>G	ENSP00000506251.1:n.10238C>G
ENST00000680887.1:c.10230C>G	ENSP00000505508.1:p.Asp3410Glu
ENST00000380152.7:c.10230C>G	ENSP00000369497.3:p.Asp3410Glu
ENST00000544455.5:c.10230C>G	ENSP00000439902.1:p.Asp3410Glu
NM_000059.3:c.10230C>G , LRG_293t1:c.10230C>G	NP_000050.2:p.Asp3410Glu
XM_011535203.1:c.10230C>G	XP_011533505.1:p.Asp3410Glu
XM_011535204.1:c.10134C>G	XP_011533506.1:p.Asp3378Glu
NM_000059.4:c.10230C>G MANE Select	NP_000050.3:p.Asp3410Glu