Canonical Allele Identifier: CA16619791

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32394926C>G , CM000675.2:g.32394926C>G	GRCh38
NC_000013.10:g.32969063C>G , CM000675.1:g.32969063C>G	GRCh37
NC_000013.9:g.31867063C>G	NCBI36
NG_012772.3:g.84447C>G , LRG_293:g.84447C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000059.4:c.9494C>G MANE Select	NP_000050.3:p.Thr3165Ser
ENST00000380152.8:c.9494C>G MANE Select	ENSP00000369497.3:p.Thr3165Ser
NM_000059.3:c.9494C>G , LRG_293t1:c.9494C>G	NP_000050.2:p.Thr3165Ser
ENST00000380152.7:c.9494C>G	ENSP00000369497.3:p.Thr3165Ser
ENST00000470094.1:c.451C>G
ENST00000470094.2:c.9494C>G	ENSP00000434898.2:p.Thr3165Ser
ENST00000528762.2:c.*861C>G	ENSP00000433168.2:n.*861C>G
ENST00000530893.7:c.9125C>G	ENSP00000499438.2:p.Thr3042Ser
ENST00000544455.5:c.9494C>G	ENSP00000439902.1:p.Thr3165Ser
ENST00000544455.6:c.9494C>G	ENSP00000439902.1:p.Thr3165Ser
ENST00000614259.2:c.9502C>G	ENSP00000506251.1:n.9502C>G
ENST00000665585.1:c.2372C>G
ENST00000665585.2:c.*1056C>G	ENSP00000499570.2:n.*1056C>G
ENST00000666593.1:c.516C>G	ENSP00000499256.1:n.516C>G
ENST00000666593.2:c.*339C>G	ENSP00000499256.2:n.*339C>G
ENST00000680887.1:c.9494C>G	ENSP00000505508.1:p.Thr3165Ser
ENST00000700202.1:c.1910C>G	ENSP00000514856.1:p.Thr637Ser
ENST00000700202.2:c.9443C>G	ENSP00000514856.2:p.Thr3148Ser
ENST00000700203.1:n.1621C>G
XM_011535203.1:c.9494C>G	XP_011533505.1:p.Thr3165Ser
XM_011535204.1:c.9398C>G	XP_011533506.1:p.Thr3133Ser