Canonical Allele Identifier: CA387761770

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32394905C>T , CM000675.2:g.32394905C>T	GRCh38
NC_000013.10:g.32969042C>T , CM000675.1:g.32969042C>T	GRCh37
NC_000013.9:g.31867042C>T	NCBI36
NG_012772.3:g.84426C>T , LRG_293:g.84426C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000059.4:c.9473C>T MANE Select	NP_000050.3:p.Thr3158Ile
ENST00000380152.8:c.9473C>T MANE Select	ENSP00000369497.3:p.Thr3158Ile
NM_000059.3:c.9473C>T , LRG_293t1:c.9473C>T	NP_000050.2:p.Thr3158Ile
ENST00000380152.7:c.9473C>T	ENSP00000369497.3:p.Thr3158Ile
ENST00000470094.1:c.430C>T
ENST00000470094.2:c.9473C>T	ENSP00000434898.2:p.Thr3158Ile
ENST00000528762.2:c.*840C>T	ENSP00000433168.2:n.*840C>T
ENST00000530893.7:c.9104C>T	ENSP00000499438.2:p.Thr3035Ile
ENST00000544455.5:c.9473C>T	ENSP00000439902.1:p.Thr3158Ile
ENST00000544455.6:c.9473C>T	ENSP00000439902.1:p.Thr3158Ile
ENST00000614259.2:c.9481C>T	ENSP00000506251.1:n.9481C>T
ENST00000665585.1:c.2351C>T
ENST00000665585.2:c.*1035C>T	ENSP00000499570.2:n.*1035C>T
ENST00000666593.1:c.495C>T	ENSP00000499256.1:n.495C>T
ENST00000666593.2:c.*318C>T	ENSP00000499256.2:n.*318C>T
ENST00000680887.1:c.9473C>T	ENSP00000505508.1:p.Thr3158Ile
ENST00000700202.1:c.1889C>T	ENSP00000514856.1:p.Thr630Ile
ENST00000700202.2:c.9422C>T	ENSP00000514856.2:p.Thr3141Ile
ENST00000700203.1:n.1600C>T
XM_011535203.1:c.9473C>T	XP_011533505.1:p.Thr3158Ile
XM_011535204.1:c.9377C>T	XP_011533506.1:p.Thr3126Ile