Canonical Allele Identifier: CA2082836329

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398497_32398498delinsCA , CM000675.2:g.32398497_32398498delinsCA	GRCh38
NC_000013.10:g.32972634_32972635delinsCA , CM000675.1:g.32972634_32972635delinsCA	GRCh37
NC_000013.9:g.31870634_31870635delinsCA	NCBI36
NG_012772.3:g.88018_88019delinsCA , LRG_293:g.88018_88019delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.*507_*508delinsCA	ENSP00000434898.2:n.*507_*508delinsCA
ENST00000528762.2:c.*1351_*1352delinsCA	ENSP00000433168.2:n.*1351_*1352delinsCA
ENST00000530893.7:c.9615_9616delinsCA	ENSP00000499438.2:p.Phe3205=
ENST00000665585.2:c.*1546_*1547delinsCA	ENSP00000499570.2:n.*1546_*1547delinsCA
ENST00000700202.2:c.9933_9934delinsCA	ENSP00000514856.2:p.Phe3311=
ENST00000700202.1:c.2400_2401delinsCA	ENSP00000514856.1:p.Phe800=
ENST00000700203.1:n.2111_2112delinsCA
ENST00000380152.8:c.9984_9985delinsCA MANE Select	ENSP00000369497.3:p.Phe3328=
ENST00000544455.6:c.9984_9985delinsCA	ENSP00000439902.1:p.Phe3328=
ENST00000614259.2:c.9992_9993delinsCA	ENSP00000506251.1:n.9992_9993delinsCA
ENST00000680887.1:c.9984_9985delinsCA	ENSP00000505508.1:p.Phe3328=
ENST00000380152.7:c.9984_9985delinsCA	ENSP00000369497.3:p.Phe3328=
ENST00000544455.5:c.9984_9985delinsCA	ENSP00000439902.1:p.Phe3328=
NM_000059.3:c.9984_9985delinsCA , LRG_293t1:c.9984_9985delinsCA	NP_000050.2:p.Phe3328=
XM_011535203.1:c.9984_9985delinsCA	XP_011533505.1:p.Phe3328=
XM_011535204.1:c.9888_9889delinsCA	XP_011533506.1:p.Phe3296=
NM_000059.4:c.9984_9985delinsCA MANE Select	NP_000050.3:p.Phe3328=