Canonical Allele Identifier: CA2622572519

Gene: BRCA2

Linked Data

• gnomAD v4: 13-32362415-TTAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32362417_32362419del , CM000675.2:g.32362417_32362419del	GRCh38
NC_000013.10:g.32936554_32936556del , CM000675.1:g.32936554_32936556del	GRCh37
NC_000013.9:g.31834554_31834556del	NCBI36
NG_012772.3:g.51938_51940del , LRG_293:g.51938_51940del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7806-106_7806-104del	ENSP00000434898.2:n.7806-106_7806-104del
ENST00000528762.2:c.7806-106_7806-104del	ENSP00000433168.2:n.7806-106_7806-104del
ENST00000530893.7:c.7437-106_7437-104del	ENSP00000499438.2:n.7437-106_7437-104del
ENST00000665585.2:c.7806-106_7806-104del	ENSP00000499570.2:n.7806-106_7806-104del
ENST00000666593.2:c.7806-106_7806-104del	ENSP00000499256.2:n.7806-106_7806-104del
ENST00000700202.2:c.7806-106_7806-104del	ENSP00000514856.2:n.7806-106_7806-104del
ENST00000700202.1:c.273-106_273-104del	ENSP00000514856.1:n.273-106_273-104del
ENST00000380152.8:c.7806-106_7806-104del MANE Select	ENSP00000369497.3:n.7806-106_7806-104del
ENST00000544455.6:c.7806-106_7806-104del	ENSP00000439902.1:n.7806-106_7806-104del
ENST00000614259.2:c.7806-98_7806-96del	ENSP00000506251.1:n.7806-98_7806-96del
ENST00000665585.1:c.371-106_371-104del
ENST00000680887.1:c.7806-106_7806-104del	ENSP00000505508.1:n.7806-106_7806-104del
ENST00000380152.7:c.7806-106_7806-104del	ENSP00000369497.3:n.7806-106_7806-104del
ENST00000544455.5:c.7806-106_7806-104del	ENSP00000439902.1:n.7806-106_7806-104del
ENST00000614259.1:n.7806-98_7806-96del
NM_000059.3:c.7806-106_7806-104del , LRG_293t1:c.7806-106_7806-104del	NP_000050.2:n.7806-106_7806-104del
XM_011535203.1:c.7806-106_7806-104del	XP_011533505.1:n.7806-106_7806-104del
XM_011535204.1:c.7710-106_7710-104del	XP_011533506.1:n.7710-106_7710-104del
XM_011535205.1:c.7806-106_7806-104del	XP_011533507.1:n.7806-106_7806-104del
NM_000059.4:c.7806-106_7806-104del MANE Select	NP_000050.3:n.7806-106_7806-104del