Canonical Allele Identifier: CA2082831577

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32362632_32362633delinsCC , CM000675.2:g.32362632_32362633delinsCC	GRCh38
NC_000013.10:g.32936769_32936770delinsCC , CM000675.1:g.32936769_32936770delinsCC	GRCh37
NC_000013.9:g.31834769_31834770delinsCC	NCBI36
NG_012772.3:g.52153_52154delinsCC , LRG_293:g.52153_52154delinsCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7915_7916delinsCC	ENSP00000434898.2:p.Pro2639=
ENST00000528762.2:c.7915_7916delinsCC	ENSP00000433168.2:p.Pro2639=
ENST00000530893.7:c.7546_7547delinsCC	ENSP00000499438.2:p.Pro2516=
ENST00000665585.2:c.7915_7916delinsCC	ENSP00000499570.2:p.Pro2639=
ENST00000666593.2:c.7915_7916delinsCC	ENSP00000499256.2:p.Pro2639=
ENST00000700202.2:c.7915_7916delinsCC	ENSP00000514856.2:p.Pro2639=
ENST00000700202.1:c.382_383delinsCC	ENSP00000514856.1:p.Pro128=
ENST00000380152.8:c.7915_7916delinsCC MANE Select	ENSP00000369497.3:p.Pro2639=
ENST00000544455.6:c.7915_7916delinsCC	ENSP00000439902.1:p.Pro2639=
ENST00000614259.2:c.7923_7924delinsCC	ENSP00000506251.1:p.Phe2641=
ENST00000665585.1:c.480_481delinsCC
ENST00000680887.1:c.7915_7916delinsCC	ENSP00000505508.1:p.Pro2639=
ENST00000380152.7:c.7915_7916delinsCC	ENSP00000369497.3:p.Pro2639=
ENST00000544455.5:c.7915_7916delinsCC	ENSP00000439902.1:p.Pro2639=
ENST00000614259.1:n.7923_7924delinsCC
NM_000059.3:c.7915_7916delinsCC , LRG_293t1:c.7915_7916delinsCC	NP_000050.2:p.Pro2639=
XM_011535203.1:c.7915_7916delinsCC	XP_011533505.1:p.Pro2639=
XM_011535204.1:c.7819_7820delinsCC	XP_011533506.1:p.Pro2607=
XM_011535205.1:c.7915_7916delinsCC	XP_011533507.1:p.Pro2639=
NM_000059.4:c.7915_7916delinsCC MANE Select	NP_000050.3:p.Pro2639=