Canonical Allele Identifier: CA609091787

Gene: BRCA2

Linked Data

• dbSNP Id: rs1269684078
• gnomAD v2: 13-32936543-CAT-C
• gnomAD v3: 13-32362406-CAT-C
• gnomAD v4: 13-32362406-CAT-C
• MyVariant Identifiers: chr13:g.32936544_32936545del (hg19) ; chr13:g.32362407_32362408del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32362408_32362409del , CM000675.2:g.32362408_32362409del	GRCh38
NC_000013.10:g.32936545_32936546del , CM000675.1:g.32936545_32936546del	GRCh37
NC_000013.9:g.31834545_31834546del	NCBI36
NG_012772.3:g.51929_51930del , LRG_293:g.51929_51930del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7806-115_7806-114del	ENSP00000434898.2:n.7806-115_7806-114del
ENST00000528762.2:c.7806-115_7806-114del	ENSP00000433168.2:n.7806-115_7806-114del
ENST00000530893.7:c.7437-115_7437-114del	ENSP00000499438.2:n.7437-115_7437-114del
ENST00000665585.2:c.7806-115_7806-114del	ENSP00000499570.2:n.7806-115_7806-114del
ENST00000666593.2:c.7806-115_7806-114del	ENSP00000499256.2:n.7806-115_7806-114del
ENST00000700202.2:c.7806-115_7806-114del	ENSP00000514856.2:n.7806-115_7806-114del
ENST00000700202.1:c.273-115_273-114del	ENSP00000514856.1:n.273-115_273-114del
ENST00000380152.8:c.7806-115_7806-114del MANE Select	ENSP00000369497.3:n.7806-115_7806-114del
ENST00000544455.6:c.7806-115_7806-114del	ENSP00000439902.1:n.7806-115_7806-114del
ENST00000614259.2:c.7806-107_7806-106del	ENSP00000506251.1:n.7806-107_7806-106del
ENST00000665585.1:c.371-115_371-114del
ENST00000680887.1:c.7806-115_7806-114del	ENSP00000505508.1:n.7806-115_7806-114del
ENST00000380152.7:c.7806-115_7806-114del	ENSP00000369497.3:n.7806-115_7806-114del
ENST00000544455.5:c.7806-115_7806-114del	ENSP00000439902.1:n.7806-115_7806-114del
ENST00000614259.1:n.7806-107_7806-106del
NM_000059.3:c.7806-115_7806-114del , LRG_293t1:c.7806-115_7806-114del	NP_000050.2:n.7806-115_7806-114del
XM_011535203.1:c.7806-115_7806-114del	XP_011533505.1:n.7806-115_7806-114del
XM_011535204.1:c.7710-115_7710-114del	XP_011533506.1:n.7710-115_7710-114del
XM_011535205.1:c.7806-115_7806-114del	XP_011533507.1:n.7806-115_7806-114del
NM_000059.4:c.7806-115_7806-114del MANE Select	NP_000050.3:n.7806-115_7806-114del