Canonical Allele Identifier: CA2622601587

Gene: BRCA2

Linked Data

• gnomAD v4: 13-32376537-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32376537_32376538insT , CM000675.2:g.32376537_32376538insT	GRCh38
NC_000013.10:g.32950674_32950675insT , CM000675.1:g.32950674_32950675insT	GRCh37
NC_000013.9:g.31848674_31848675insT	NCBI36
NG_012772.3:g.66058_66059insT , LRG_293:g.66058_66059insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8633-133_8633-132insT	ENSP00000434898.2:n.8633-133_8633-132insT
ENST00000528762.2:c.8697-133_8697-132insT	ENSP00000433168.2:n.8697-133_8697-132insT
ENST00000530893.7:c.8264-133_8264-132insT	ENSP00000499438.2:n.8264-133_8264-132insT
ENST00000665585.2:c.*195-133_*195-132insT	ENSP00000499570.2:n.*195-133_*195-132insT
ENST00000666593.2:c.8633-133_8633-132insT	ENSP00000499256.2:n.8633-133_8633-132insT
ENST00000700202.2:c.8633-133_8633-132insT	ENSP00000514856.2:n.8633-133_8633-132insT
ENST00000700202.1:c.1100-133_1100-132insT	ENSP00000514856.1:n.1100-133_1100-132insT
ENST00000700203.1:n.627_628insT
ENST00000380152.8:c.8633-133_8633-132insT MANE Select	ENSP00000369497.3:n.8633-133_8633-132insT
ENST00000544455.6:c.8633-133_8633-132insT	ENSP00000439902.1:n.8633-133_8633-132insT
ENST00000614259.2:c.8641-133_8641-132insT	ENSP00000506251.1:n.8641-133_8641-132insT
ENST00000665585.1:c.1511-133_1511-132insT
ENST00000680887.1:c.8633-133_8633-132insT	ENSP00000505508.1:n.8633-133_8633-132insT
ENST00000380152.7:c.8633-133_8633-132insT	ENSP00000369497.3:n.8633-133_8633-132insT
ENST00000528762.1:c.195-133_195-132insT	ENSP00000433168.1:n.195-133_195-132insT
ENST00000544455.5:c.8633-133_8633-132insT	ENSP00000439902.1:n.8633-133_8633-132insT
NM_000059.3:c.8633-133_8633-132insT , LRG_293t1:c.8633-133_8633-132insT	NP_000050.2:n.8633-133_8633-132insT
XM_011535203.1:c.8633-133_8633-132insT	XP_011533505.1:n.8633-133_8633-132insT
XM_011535204.1:c.8537-133_8537-132insT	XP_011533506.1:n.8537-133_8537-132insT
XM_011535205.1:c.8633-133_8633-132insT	XP_011533507.1:n.8633-133_8633-132insT
NM_000059.4:c.8633-133_8633-132insT MANE Select	NP_000050.3:n.8633-133_8633-132insT