Canonical Allele Identifier: CA2082810551

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32338672_32338674delinsCAA , CM000675.2:g.32338672_32338674delinsCAA	GRCh38
NC_000013.10:g.32912809_32912811delinsCAA , CM000675.1:g.32912809_32912811delinsCAA	GRCh37
NC_000013.9:g.31810809_31810811delinsCAA	NCBI36
NG_012772.3:g.28193_28195delinsCAA , LRG_293:g.28193_28195delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.4317_4319delinsCAA	ENSP00000434898.2:p.Ala1439=
ENST00000528762.2:c.4317_4319delinsCAA	ENSP00000433168.2:p.Ala1439=
ENST00000530893.7:c.3948_3950delinsCAA	ENSP00000499438.2:p.Ala1316=
ENST00000665585.2:c.4317_4319delinsCAA	ENSP00000499570.2:p.Ala1439=
ENST00000666593.2:c.4317_4319delinsCAA	ENSP00000499256.2:p.Ala1439=
ENST00000700202.2:c.4317_4319delinsCAA	ENSP00000514856.2:p.Ala1439=
ENST00000380152.8:c.4317_4319delinsCAA MANE Select	ENSP00000369497.3:p.Ala1439=
ENST00000544455.6:c.4317_4319delinsCAA	ENSP00000439902.1:p.Ala1439=
ENST00000614259.2:c.4317_4319delinsCAA	ENSP00000506251.1:p.Ala1439=
ENST00000680887.1:c.4317_4319delinsCAA	ENSP00000505508.1:p.Ala1439=
ENST00000380152.7:c.4317_4319delinsCAA	ENSP00000369497.3:p.Ala1439=
ENST00000544455.5:c.4317_4319delinsCAA	ENSP00000439902.1:p.Ala1439=
ENST00000614259.1:n.4317_4319delinsCAA
NM_000059.3:c.4317_4319delinsCAA , LRG_293t1:c.4317_4319delinsCAA	NP_000050.2:p.Ala1439=
XM_011535203.1:c.4317_4319delinsCAA	XP_011533505.1:p.Ala1439=
XM_011535204.1:c.4317_4319delinsCAA	XP_011533506.1:p.Ala1439=
XM_011535205.1:c.4317_4319delinsCAA	XP_011533507.1:p.Ala1439=
NM_000059.4:c.4317_4319delinsCAA MANE Select	NP_000050.3:p.Ala1439=