Canonical Allele Identifier: CA387766571

Gene: BRCA2

Linked Data

• MyVariant Identifiers: chr13:g.32972510G>T (hg19) ; chr13:g.32398373G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398373G>T , CM000675.2:g.32398373G>T	GRCh38
NC_000013.10:g.32972510G>T , CM000675.1:g.32972510G>T	GRCh37
NC_000013.9:g.31870510G>T	NCBI36
NG_012772.3:g.87894G>T , LRG_293:g.87894G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*383G>T	ENSP00000434898.2:n.*383G>T
ENST00000528762.2:c.*1227G>T	ENSP00000433168.2:n.*1227G>T
ENST00000530893.7:c.9491G>T	ENSP00000499438.2:p.Cys3164Phe
ENST00000665585.2:c.*1422G>T	ENSP00000499570.2:n.*1422G>T
ENST00000700202.2:c.9809G>T	ENSP00000514856.2:p.Cys3270Phe
ENST00000700202.1:c.2276G>T	ENSP00000514856.1:p.Cys759Phe
ENST00000700203.1:n.1987G>T
ENST00000380152.8:c.9860G>T MANE Select	ENSP00000369497.3:p.Cys3287Phe
ENST00000544455.6:c.9860G>T	ENSP00000439902.1:p.Cys3287Phe
ENST00000614259.2:c.9868G>T	ENSP00000506251.1:n.9868G>T
ENST00000680887.1:c.9860G>T	ENSP00000505508.1:p.Cys3287Phe
ENST00000380152.7:c.9860G>T	ENSP00000369497.3:p.Cys3287Phe
ENST00000533776.1:n.448G>T
ENST00000544455.5:c.9860G>T	ENSP00000439902.1:p.Cys3287Phe
NM_000059.3:c.9860G>T , LRG_293t1:c.9860G>T	NP_000050.2:p.Cys3287Phe
XM_011535203.1:c.9860G>T	XP_011533505.1:p.Cys3287Phe
XM_011535204.1:c.9764G>T	XP_011533506.1:p.Cys3255Phe
NM_000059.4:c.9860G>T MANE Select	NP_000050.3:p.Cys3287Phe