Canonical Allele Identifier: CA2082829827

Gene: BRCA2

Linked Data

• dbSNP Id: rs2072743194
• gnomAD v4: 13-32362414-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32362415_32362416del , CM000675.2:g.32362415_32362416del	GRCh38
NC_000013.10:g.32936552_32936553del , CM000675.1:g.32936552_32936553del	GRCh37
NC_000013.9:g.31834552_31834553del	NCBI36
NG_012772.3:g.51936_51937del , LRG_293:g.51936_51937del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7806-108_7806-107del	ENSP00000434898.2:n.7806-108_7806-107del
ENST00000528762.2:c.7806-108_7806-107del	ENSP00000433168.2:n.7806-108_7806-107del
ENST00000530893.7:c.7437-108_7437-107del	ENSP00000499438.2:n.7437-108_7437-107del
ENST00000665585.2:c.7806-108_7806-107del	ENSP00000499570.2:n.7806-108_7806-107del
ENST00000666593.2:c.7806-108_7806-107del	ENSP00000499256.2:n.7806-108_7806-107del
ENST00000700202.2:c.7806-108_7806-107del	ENSP00000514856.2:n.7806-108_7806-107del
ENST00000700202.1:c.273-108_273-107del	ENSP00000514856.1:n.273-108_273-107del
ENST00000380152.8:c.7806-108_7806-107del MANE Select	ENSP00000369497.3:n.7806-108_7806-107del
ENST00000544455.6:c.7806-108_7806-107del	ENSP00000439902.1:n.7806-108_7806-107del
ENST00000614259.2:c.7806-100_7806-99del	ENSP00000506251.1:n.7806-100_7806-99del
ENST00000665585.1:c.371-108_371-107del
ENST00000680887.1:c.7806-108_7806-107del	ENSP00000505508.1:n.7806-108_7806-107del
ENST00000380152.7:c.7806-108_7806-107del	ENSP00000369497.3:n.7806-108_7806-107del
ENST00000544455.5:c.7806-108_7806-107del	ENSP00000439902.1:n.7806-108_7806-107del
ENST00000614259.1:n.7806-100_7806-99del
NM_000059.3:c.7806-108_7806-107del , LRG_293t1:c.7806-108_7806-107del	NP_000050.2:n.7806-108_7806-107del
XM_011535203.1:c.7806-108_7806-107del	XP_011533505.1:n.7806-108_7806-107del
XM_011535204.1:c.7710-108_7710-107del	XP_011533506.1:n.7710-108_7710-107del
XM_011535205.1:c.7806-108_7806-107del	XP_011533507.1:n.7806-108_7806-107del
NM_000059.4:c.7806-108_7806-107del MANE Select	NP_000050.3:n.7806-108_7806-107del