Canonical Allele Identifier: CA2573149291

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 1451504
• ClinVar RCV Id: RCV001993269
• dbSNP Id: rs1555283980

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32339248_32339249del , CM000675.2:g.32339248_32339249del	GRCh38
NC_000013.10:g.32913385_32913386del , CM000675.1:g.32913385_32913386del	GRCh37
NC_000013.9:g.31811385_31811386del	NCBI36
NG_012772.3:g.28769_28770del , LRG_293:g.28769_28770del

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.4893_4894del	ENSP00000434898.2:p.Ser1632TyrfsTer6
ENST00000528762.2:c.4893_4894del	ENSP00000433168.2:p.Ser1632TyrfsTer6
ENST00000530893.7:c.4524_4525del	ENSP00000499438.2:p.Ser1509TyrfsTer6
ENST00000665585.2:c.4893_4894del	ENSP00000499570.2:p.Ser1632TyrfsTer6
ENST00000666593.2:c.4893_4894del	ENSP00000499256.2:p.Ser1632TyrfsTer6
ENST00000700202.2:c.4893_4894del	ENSP00000514856.2:p.Ser1632TyrfsTer6
ENST00000380152.8:c.4893_4894del MANE Select	ENSP00000369497.3:p.Ser1632TyrfsTer6
ENST00000544455.6:c.4893_4894del	ENSP00000439902.1:p.Ser1632TyrfsTer6
ENST00000614259.2:c.4893_4894del	ENSP00000506251.1:p.Ser1632TyrfsTer6
ENST00000680887.1:c.4893_4894del	ENSP00000505508.1:p.Ser1632TyrfsTer6
ENST00000380152.7:c.4893_4894del	ENSP00000369497.3:p.Ser1632TyrfsTer6
ENST00000544455.5:c.4893_4894del	ENSP00000439902.1:p.Ser1632TyrfsTer6
ENST00000614259.1:n.4893_4894del
NM_000059.3:c.4893_4894del , LRG_293t1:c.4893_4894del	NP_000050.2:p.Ser1632TyrfsTer6
XM_011535203.1:c.4893_4894del	XP_011533505.1:p.Ser1632TyrfsTer6
XM_011535204.1:c.4893_4894del	XP_011533506.1:p.Ser1632TyrfsTer6
XM_011535205.1:c.4893_4894del	XP_011533507.1:p.Ser1632TyrfsTer6
NM_000059.4:c.4893_4894del MANE Select	NP_000050.3:p.Ser1632TyrfsTer6