Canonical Allele Identifier: CA025737

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 52636
• ClinVar RCV Id: RCV000113970 ; RCV000218194 ; RCV001390828 ; RCV003162392
• dbSNP Id: rs80359121
• MyVariant Identifiers: chr13:g.32945234G>T (hg19) ; chr13:g.32371097G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32371097G>T , CM000675.2:g.32371097G>T	GRCh38
NC_000013.10:g.32945234G>T , CM000675.1:g.32945234G>T	GRCh37
NC_000013.9:g.31843234G>T	NCBI36
NG_012772.3:g.60618G>T , LRG_293:g.60618G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8629G>T	ENSP00000434898.2:p.Glu2877Ter
ENST00000528762.2:c.8629G>T	ENSP00000433168.2:p.Glu2877Ter
ENST00000530893.7:c.8260G>T	ENSP00000499438.2:p.Glu2754Ter
ENST00000665585.2:c.8629G>T	ENSP00000499570.2:p.Glu2877Ter
ENST00000666593.2:c.8629G>T	ENSP00000499256.2:p.Glu2877Ter
ENST00000700202.2:c.8629G>T	ENSP00000514856.2:p.Glu2877Ter
ENST00000700202.1:c.1096G>T	ENSP00000514856.1:p.Glu366Ter
ENST00000380152.8:c.8629G>T MANE Select	ENSP00000369497.3:p.Glu2877Ter
ENST00000544455.6:c.8629G>T	ENSP00000439902.1:p.Glu2877Ter
ENST00000614259.2:c.8637G>T	ENSP00000506251.1:n.8637G>T
ENST00000665585.1:c.1194G>T
ENST00000680887.1:c.8629G>T	ENSP00000505508.1:p.Glu2877Ter
ENST00000380152.7:c.8629G>T	ENSP00000369497.3:p.Glu2877Ter
ENST00000528762.1:c.127G>T	ENSP00000433168.1:p.Glu43Ter
ENST00000544455.5:c.8629G>T	ENSP00000439902.1:p.Glu2877Ter
NM_000059.3:c.8629G>T , LRG_293t1:c.8629G>T	NP_000050.2:p.Glu2877Ter
XM_011535203.1:c.8629G>T	XP_011533505.1:p.Glu2877Ter
XM_011535204.1:c.8533G>T	XP_011533506.1:p.Glu2845Ter
XM_011535205.1:c.8629G>T	XP_011533507.1:p.Glu2877Ter
NM_000059.4:c.8629G>T MANE Select	NP_000050.3:p.Glu2877Ter