Canonical Allele Identifier: CA387768112

Gene: BRCA2

Linked Data

• MyVariant Identifiers: chr13:g.32972785T>G (hg19) ; chr13:g.32398648T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398648T>G , CM000675.2:g.32398648T>G	GRCh38
NC_000013.10:g.32972785T>G , CM000675.1:g.32972785T>G	GRCh37
NC_000013.9:g.31870785T>G	NCBI36
NG_012772.3:g.88169T>G , LRG_293:g.88169T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.*658T>G	ENSP00000434898.2:n.*658T>G
ENST00000528762.2:c.*1502T>G	ENSP00000433168.2:n.*1502T>G
ENST00000530893.7:c.9766T>G	ENSP00000499438.2:p.Tyr3256Asp
ENST00000665585.2:c.*1697T>G	ENSP00000499570.2:n.*1697T>G
ENST00000700202.2:c.10084T>G	ENSP00000514856.2:p.Tyr3362Asp
ENST00000700202.1:c.2551T>G	ENSP00000514856.1:p.Tyr851Asp
ENST00000700203.1:n.2262T>G
ENST00000380152.8:c.10135T>G MANE Select	ENSP00000369497.3:p.Tyr3379Asp
ENST00000544455.6:c.10135T>G	ENSP00000439902.1:p.Tyr3379Asp
ENST00000614259.2:c.10143T>G	ENSP00000506251.1:n.10143T>G
ENST00000680887.1:c.10135T>G	ENSP00000505508.1:p.Tyr3379Asp
ENST00000380152.7:c.10135T>G	ENSP00000369497.3:p.Tyr3379Asp
ENST00000544455.5:c.10135T>G	ENSP00000439902.1:p.Tyr3379Asp
NM_000059.3:c.10135T>G , LRG_293t1:c.10135T>G	NP_000050.2:p.Tyr3379Asp
XM_011535203.1:c.10135T>G	XP_011533505.1:p.Tyr3379Asp
XM_011535204.1:c.10039T>G	XP_011533506.1:p.Tyr3347Asp
NM_000059.4:c.10135T>G MANE Select	NP_000050.3:p.Tyr3379Asp