Canonical Allele Identifier: CA387761356

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32394830C>G , CM000675.2:g.32394830C>G	GRCh38
NC_000013.10:g.32968967C>G , CM000675.1:g.32968967C>G	GRCh37
NC_000013.9:g.31866967C>G	NCBI36
NG_012772.3:g.84351C>G , LRG_293:g.84351C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000059.4:c.9398C>G MANE Select	NP_000050.3:p.Ser3133Ter
ENST00000380152.8:c.9398C>G MANE Select	ENSP00000369497.3:p.Ser3133Ter
NM_000059.3:c.9398C>G , LRG_293t1:c.9398C>G	NP_000050.2:p.Ser3133Ter
ENST00000380152.7:c.9398C>G	ENSP00000369497.3:p.Ser3133Ter
ENST00000470094.1:c.355C>G
ENST00000470094.2:c.9398C>G	ENSP00000434898.2:p.Ser3133Ter
ENST00000528762.2:c.*765C>G	ENSP00000433168.2:n.*765C>G
ENST00000530893.7:c.9029C>G	ENSP00000499438.2:p.Ser3010Ter
ENST00000544455.5:c.9398C>G	ENSP00000439902.1:p.Ser3133Ter
ENST00000544455.6:c.9398C>G	ENSP00000439902.1:p.Ser3133Ter
ENST00000614259.2:c.9406C>G	ENSP00000506251.1:n.9406C>G
ENST00000665585.1:c.2276C>G
ENST00000665585.2:c.*960C>G	ENSP00000499570.2:n.*960C>G
ENST00000666593.1:c.420C>G	ENSP00000499256.1:n.420C>G
ENST00000666593.2:c.*243C>G	ENSP00000499256.2:n.*243C>G
ENST00000680887.1:c.9398C>G	ENSP00000505508.1:p.Ser3133Ter
ENST00000700202.1:c.1814C>G	ENSP00000514856.1:p.Ser605Ter
ENST00000700202.2:c.9347C>G	ENSP00000514856.2:p.Ser3116Ter
ENST00000700203.1:n.1525C>G
XM_011535203.1:c.9398C>G	XP_011533505.1:p.Ser3133Ter
XM_011535204.1:c.9302C>G	XP_011533506.1:p.Ser3101Ter