Canonical Allele Identifier: CA2082835215

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32363288_32363304delinsTTGAGCGCAAATATATC , CM000675.2:g.32363288_32363304delinsTTGAGCGCAAATATATC	GRCh38
NC_000013.10:g.32937425_32937441delinsTTGAGCGCAAATATATC , CM000675.1:g.32937425_32937441delinsTTGAGCGCAAATATATC	GRCh37
NC_000013.9:g.31835425_31835441delinsTTGAGCGCAAATATATC	NCBI36
NG_012772.3:g.52809_52825delinsTTGAGCGCAAATATATC , LRG_293:g.52809_52825delinsTTGAGCGCAAATATATC

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.8086_8102delinsTTGAGCGCAAATATATC	ENSP00000434898.2:p.Leu2696=
ENST00000528762.2:c.8086_8102delinsTTGAGCGCAAATATATC	ENSP00000433168.2:p.Leu2696=
ENST00000530893.7:c.7717_7733delinsTTGAGCGCAAATATATC	ENSP00000499438.2:p.Leu2573=
ENST00000665585.2:c.8086_8102delinsTTGAGCGCAAATATATC	ENSP00000499570.2:p.Leu2696=
ENST00000666593.2:c.8086_8102delinsTTGAGCGCAAATATATC	ENSP00000499256.2:p.Leu2696=
ENST00000700202.2:c.8086_8102delinsTTGAGCGCAAATATATC	ENSP00000514856.2:p.Leu2696=
ENST00000700202.1:c.553_569delinsTTGAGCGCAAATATATC	ENSP00000514856.1:p.Leu185=
ENST00000380152.8:c.8086_8102delinsTTGAGCGCAAATATATC MANE Select	ENSP00000369497.3:p.Leu2696=
ENST00000544455.6:c.8086_8102delinsTTGAGCGCAAATATATC	ENSP00000439902.1:p.Leu2696=
ENST00000614259.2:c.8094_8110delinsTTGAGCGCAAATATATC	ENSP00000506251.1:n.8094_8110delinsTTGAGC...
ENST00000665585.1:c.651_667delinsTTGAGCGCAAATATATC
ENST00000680887.1:c.8086_8102delinsTTGAGCGCAAATATATC	ENSP00000505508.1:p.Leu2696=
ENST00000380152.7:c.8086_8102delinsTTGAGCGCAAATATATC	ENSP00000369497.3:p.Leu2696=
ENST00000544455.5:c.8086_8102delinsTTGAGCGCAAATATATC	ENSP00000439902.1:p.Leu2696=
NM_000059.3:c.8086_8102delinsTTGAGCGCAAATATATC , LRG_293t1:c.8086_8102delinsTTGAGCGCAAATATATC	NP_000050.2:p.Leu2696=
XM_011535203.1:c.8086_8102delinsTTGAGCGCAAATATATC	XP_011533505.1:p.Leu2696=
XM_011535204.1:c.7990_8006delinsTTGAGCGCAAATATATC	XP_011533506.1:p.Leu2664=
XM_011535205.1:c.8086_8102delinsTTGAGCGCAAATATATC	XP_011533507.1:p.Leu2696=
NM_000059.4:c.8086_8102delinsTTGAGCGCAAATATATC MANE Select	NP_000050.3:p.Leu2696=