Canonical Allele Identifier: CA1139663135

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 962398
• ClinVar RCV Id: RCV001236249
• dbSNP Id: rs2072471826

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32337435_32337462del , CM000675.2:g.32337435_32337462del	GRCh38
NC_000013.10:g.32911572_32911599del , CM000675.1:g.32911572_32911599del	GRCh37
NC_000013.9:g.31809572_31809599del	NCBI36
NG_012772.3:g.26956_26983del , LRG_293:g.26956_26983del

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.3080_3107del	ENSP00000434898.2:p.Ser1027AsnfsTer7
ENST00000528762.2:c.3080_3107del	ENSP00000433168.2:p.Ser1027AsnfsTer7
ENST00000530893.7:c.2711_2738del	ENSP00000499438.2:p.Ser904AsnfsTer7
ENST00000665585.2:c.3080_3107del	ENSP00000499570.2:p.Ser1027AsnfsTer7
ENST00000666593.2:c.3080_3107del	ENSP00000499256.2:p.Ser1027AsnfsTer7
ENST00000700202.2:c.3080_3107del	ENSP00000514856.2:p.Ser1027AsnfsTer7
ENST00000380152.8:c.3080_3107del MANE Select	ENSP00000369497.3:p.Ser1027AsnfsTer7
ENST00000544455.6:c.3080_3107del	ENSP00000439902.1:p.Ser1027AsnfsTer7
ENST00000614259.2:c.3080_3107del	ENSP00000506251.1:p.Ser1027AsnfsTer7
ENST00000680887.1:c.3080_3107del	ENSP00000505508.1:p.Ser1027AsnfsTer7
ENST00000380152.7:c.3080_3107del	ENSP00000369497.3:p.Ser1027AsnfsTer7
ENST00000544455.5:c.3080_3107del	ENSP00000439902.1:p.Ser1027AsnfsTer7
ENST00000614259.1:n.3080_3107del
NM_000059.3:c.3080_3107del , LRG_293t1:c.3080_3107del	NP_000050.2:p.Ser1027AsnfsTer7
XM_011535203.1:c.3080_3107del	XP_011533505.1:p.Ser1027AsnfsTer7
XM_011535204.1:c.3080_3107del	XP_011533506.1:p.Ser1027AsnfsTer7
XM_011535205.1:c.3080_3107del	XP_011533507.1:p.Ser1027AsnfsTer7
NM_000059.4:c.3080_3107del MANE Select	NP_000050.3:p.Ser1027AsnfsTer7