Canonical Allele Identifier: CA697324889

Gene: BRCA2

Linked Data

• dbSNP Id: rs1415954807
• MyVariant Identifiers: chr13:g.32890711del (hg19) ; chr13:g.32316574del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32316577del , CM000675.2:g.32316577del	GRCh38
NC_000013.10:g.32890714del , CM000675.1:g.32890714del	GRCh37
NC_000013.9:g.31788714del	NCBI36
NG_012772.3:g.6098del , LRG_293:g.6098del
NG_017006.1:g.381del
NG_017006.2:g.3790del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.67+50del	ENSP00000434898.2:n.67+50del
ENST00000528762.2:c.67+50del	ENSP00000433168.2:n.67+50del
ENST00000530893.7:c.-303+54del	ENSP00000499438.2:n.-303+54del
ENST00000665585.2:c.67+50del	ENSP00000499570.2:n.67+50del
ENST00000666593.2:c.67+50del	ENSP00000499256.2:n.67+50del
ENST00000700202.2:c.67+50del	ENSP00000514856.2:n.67+50del
ENST00000700199.1:n.241del
ENST00000700200.1:n.191+50del
ENST00000700201.1:c.67+50del	ENSP00000514855.1:n.67+50del
ENST00000380152.8:c.67+50del MANE Select	ENSP00000369497.3:n.67+50del
ENST00000544455.6:c.67+50del	ENSP00000439902.1:n.67+50del
ENST00000614259.2:c.67+50del	ENSP00000506251.1:n.67+50del
ENST00000680887.1:c.67+50del	ENSP00000505508.1:n.67+50del
ENST00000380152.7:c.67+50del	ENSP00000369497.3:n.67+50del
ENST00000530893.6:n.265+54del
ENST00000544455.5:c.67+50del	ENSP00000439902.1:n.67+50del
ENST00000614259.1:n.67+50del
NM_000059.3:c.67+50del , LRG_293t1:c.67+50del	NP_000050.2:n.67+50del
XM_011535203.1:c.67+50del	XP_011533505.1:n.67+50del
XM_011535204.1:c.67+50del	XP_011533506.1:n.67+50del
XM_011535205.1:c.67+50del	XP_011533507.1:n.67+50del
NM_000059.4:c.67+50del MANE Select	NP_000050.3:n.67+50del