Canonical Allele Identifier: CA387757982

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32380055C>T , CM000675.2:g.32380055C>T	GRCh38
NC_000013.10:g.32954192C>T , CM000675.1:g.32954192C>T	GRCh37
NC_000013.9:g.31852192C>T	NCBI36
NG_012772.3:g.69576C>T , LRG_293:g.69576C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000059.4:c.9166C>T MANE Select	NP_000050.3:p.His3056Tyr
ENST00000380152.8:c.9166C>T MANE Select	ENSP00000369497.3:p.His3056Tyr
NM_000059.3:c.9166C>T , LRG_293t1:c.9166C>T	NP_000050.2:p.His3056Tyr
ENST00000380152.7:c.9166C>T	ENSP00000369497.3:p.His3056Tyr
ENST00000470094.1:c.123C>T
ENST00000470094.2:c.9166C>T	ENSP00000434898.2:p.His3056Tyr
ENST00000528762.2:c.*533C>T	ENSP00000433168.2:n.*533C>T
ENST00000530893.7:c.8797C>T	ENSP00000499438.2:p.His2933Tyr
ENST00000544455.5:c.9166C>T	ENSP00000439902.1:p.His3056Tyr
ENST00000544455.6:c.9166C>T	ENSP00000439902.1:p.His3056Tyr
ENST00000614259.2:c.9174C>T	ENSP00000506251.1:n.9174C>T
ENST00000665585.1:c.2044C>T
ENST00000665585.2:c.*728C>T	ENSP00000499570.2:n.*728C>T
ENST00000666593.1:c.49C>T	ENSP00000499256.1:p.His17Tyr
ENST00000666593.2:c.9166C>T	ENSP00000499256.2:p.His3056Tyr
ENST00000680887.1:c.9166C>T	ENSP00000505508.1:p.His3056Tyr
ENST00000700202.1:c.1582C>T	ENSP00000514856.1:p.His528Tyr
ENST00000700202.2:c.9115C>T	ENSP00000514856.2:p.His3039Tyr
ENST00000700203.1:n.1293C>T
XM_011535203.1:c.9166C>T	XP_011533505.1:p.His3056Tyr
XM_011535204.1:c.9070C>T	XP_011533506.1:p.His3024Tyr