Canonical Allele Identifier: CA387754993

Gene: BRCA2

Linked Data

• MyVariant Identifiers: chr13:g.32950903A>G (hg19) ; chr13:g.32376766A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32376766A>G , CM000675.2:g.32376766A>G	GRCh38
NC_000013.10:g.32950903A>G , CM000675.1:g.32950903A>G	GRCh37
NC_000013.9:g.31848903A>G	NCBI36
NG_012772.3:g.66287A>G , LRG_293:g.66287A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8729A>G	ENSP00000434898.2:p.Asn2910Ser
ENST00000528762.2:c.*96A>G	ENSP00000433168.2:n.*96A>G
ENST00000530893.7:c.8360A>G	ENSP00000499438.2:p.Asn2787Ser
ENST00000665585.2:c.*291A>G	ENSP00000499570.2:n.*291A>G
ENST00000666593.2:c.8729A>G	ENSP00000499256.2:p.Asn2910Ser
ENST00000700202.2:c.8729A>G	ENSP00000514856.2:p.Asn2910Ser
ENST00000700202.1:c.1196A>G	ENSP00000514856.1:p.Asn399Ser
ENST00000700203.1:n.856A>G
ENST00000380152.8:c.8729A>G MANE Select	ENSP00000369497.3:p.Asn2910Ser
ENST00000544455.6:c.8729A>G	ENSP00000439902.1:p.Asn2910Ser
ENST00000614259.2:c.8737A>G	ENSP00000506251.1:n.8737A>G
ENST00000665585.1:c.1607A>G
ENST00000680887.1:c.8729A>G	ENSP00000505508.1:p.Asn2910Ser
ENST00000380152.7:c.8729A>G	ENSP00000369497.3:p.Asn2910Ser
ENST00000528762.1:c.291A>G	ENSP00000433168.1:n.291A>G
ENST00000544455.5:c.8729A>G	ENSP00000439902.1:p.Asn2910Ser
NM_000059.3:c.8729A>G , LRG_293t1:c.8729A>G	NP_000050.2:p.Asn2910Ser
XM_011535203.1:c.8729A>G	XP_011533505.1:p.Asn2910Ser
XM_011535204.1:c.8633A>G	XP_011533506.1:p.Asn2878Ser
XM_011535205.1:c.8729A>G	XP_011533507.1:p.Asn2910Ser
NM_000059.4:c.8729A>G MANE Select	NP_000050.3:p.Asn2910Ser