Canonical Allele Identifier: CA2082811582

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32337164_32337166delinsCAA , CM000675.2:g.32337164_32337166delinsCAA	GRCh38
NC_000013.10:g.32911301_32911303delinsCAA , CM000675.1:g.32911301_32911303delinsCAA	GRCh37
NC_000013.9:g.31809301_31809303delinsCAA	NCBI36
NG_012772.3:g.26685_26687delinsCAA , LRG_293:g.26685_26687delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.2809_2811delinsCAA	ENSP00000434898.2:p.Gln937=
ENST00000528762.2:c.2809_2811delinsCAA	ENSP00000433168.2:p.Gln937=
ENST00000530893.7:c.2440_2442delinsCAA	ENSP00000499438.2:p.Gln814=
ENST00000665585.2:c.2809_2811delinsCAA	ENSP00000499570.2:p.Gln937=
ENST00000666593.2:c.2809_2811delinsCAA	ENSP00000499256.2:p.Gln937=
ENST00000700202.2:c.2809_2811delinsCAA	ENSP00000514856.2:p.Gln937=
ENST00000380152.8:c.2809_2811delinsCAA MANE Select	ENSP00000369497.3:p.Gln937=
ENST00000544455.6:c.2809_2811delinsCAA	ENSP00000439902.1:p.Gln937=
ENST00000614259.2:c.2809_2811delinsCAA	ENSP00000506251.1:p.Gln937=
ENST00000680887.1:c.2809_2811delinsCAA	ENSP00000505508.1:p.Gln937=
ENST00000380152.7:c.2809_2811delinsCAA	ENSP00000369497.3:p.Gln937=
ENST00000544455.5:c.2809_2811delinsCAA	ENSP00000439902.1:p.Gln937=
ENST00000614259.1:n.2809_2811delinsCAA
NM_000059.3:c.2809_2811delinsCAA , LRG_293t1:c.2809_2811delinsCAA	NP_000050.2:p.Gln937=
XM_011535203.1:c.2809_2811delinsCAA	XP_011533505.1:p.Gln937=
XM_011535204.1:c.2809_2811delinsCAA	XP_011533506.1:p.Gln937=
XM_011535205.1:c.2809_2811delinsCAA	XP_011533507.1:p.Gln937=
NM_000059.4:c.2809_2811delinsCAA MANE Select	NP_000050.3:p.Gln937=