Canonical Allele Identifier: CA2622601572

Gene: BRCA2

Linked Data

• gnomAD v4: 13-32376529-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32376529_32376530insT , CM000675.2:g.32376529_32376530insT	GRCh38
NC_000013.10:g.32950666_32950667insT , CM000675.1:g.32950666_32950667insT	GRCh37
NC_000013.9:g.31848666_31848667insT	NCBI36
NG_012772.3:g.66050_66051insT , LRG_293:g.66050_66051insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8633-141_8633-140insT	ENSP00000434898.2:n.8633-141_8633-140insT
ENST00000528762.2:c.8697-141_8697-140insT	ENSP00000433168.2:n.8697-141_8697-140insT
ENST00000530893.7:c.8264-141_8264-140insT	ENSP00000499438.2:n.8264-141_8264-140insT
ENST00000665585.2:c.*195-141_*195-140insT	ENSP00000499570.2:n.*195-141_*195-140insT
ENST00000666593.2:c.8633-141_8633-140insT	ENSP00000499256.2:n.8633-141_8633-140insT
ENST00000700202.2:c.8633-141_8633-140insT	ENSP00000514856.2:n.8633-141_8633-140insT
ENST00000700202.1:c.1100-141_1100-140insT	ENSP00000514856.1:n.1100-141_1100-140insT
ENST00000700203.1:n.619_620insT
ENST00000380152.8:c.8633-141_8633-140insT MANE Select	ENSP00000369497.3:n.8633-141_8633-140insT
ENST00000544455.6:c.8633-141_8633-140insT	ENSP00000439902.1:n.8633-141_8633-140insT
ENST00000614259.2:c.8641-141_8641-140insT	ENSP00000506251.1:n.8641-141_8641-140insT
ENST00000665585.1:c.1511-141_1511-140insT
ENST00000680887.1:c.8633-141_8633-140insT	ENSP00000505508.1:n.8633-141_8633-140insT
ENST00000380152.7:c.8633-141_8633-140insT	ENSP00000369497.3:n.8633-141_8633-140insT
ENST00000528762.1:c.195-141_195-140insT	ENSP00000433168.1:n.195-141_195-140insT
ENST00000544455.5:c.8633-141_8633-140insT	ENSP00000439902.1:n.8633-141_8633-140insT
NM_000059.3:c.8633-141_8633-140insT , LRG_293t1:c.8633-141_8633-140insT	NP_000050.2:n.8633-141_8633-140insT
XM_011535203.1:c.8633-141_8633-140insT	XP_011533505.1:n.8633-141_8633-140insT
XM_011535204.1:c.8537-141_8537-140insT	XP_011533506.1:n.8537-141_8537-140insT
XM_011535205.1:c.8633-141_8633-140insT	XP_011533507.1:n.8633-141_8633-140insT
NM_000059.4:c.8633-141_8633-140insT MANE Select	NP_000050.3:n.8633-141_8633-140insT