Canonical Allele Identifier: CA2622601320

Gene: BRCA2

Linked Data

• gnomAD v4: 13-32371153-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32371153_32371154insC , CM000675.2:g.32371153_32371154insC	GRCh38
NC_000013.10:g.32945290_32945291insC , CM000675.1:g.32945290_32945291insC	GRCh37
NC_000013.9:g.31843290_31843291insC	NCBI36
NG_012772.3:g.60674_60675insC , LRG_293:g.60674_60675insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8632+53_8632+54insC	ENSP00000434898.2:n.8632+53_8632+54insC
ENST00000528762.2:c.8632+53_8632+54insC	ENSP00000433168.2:n.8632+53_8632+54insC
ENST00000530893.7:c.8263+53_8263+54insC	ENSP00000499438.2:n.8263+53_8263+54insC
ENST00000665585.2:c.8632+53_8632+54insC	ENSP00000499570.2:n.8632+53_8632+54insC
ENST00000666593.2:c.8632+53_8632+54insC	ENSP00000499256.2:n.8632+53_8632+54insC
ENST00000700202.2:c.8632+53_8632+54insC	ENSP00000514856.2:n.8632+53_8632+54insC
ENST00000700202.1:c.1099+53_1099+54insC	ENSP00000514856.1:n.1099+53_1099+54insC
ENST00000380152.8:c.8632+53_8632+54insC MANE Select	ENSP00000369497.3:n.8632+53_8632+54insC
ENST00000544455.6:c.8632+53_8632+54insC	ENSP00000439902.1:n.8632+53_8632+54insC
ENST00000614259.2:c.8640+53_8640+54insC	ENSP00000506251.1:n.8640+53_8640+54insC
ENST00000665585.1:c.1197+53_1197+54insC
ENST00000680887.1:c.8632+53_8632+54insC	ENSP00000505508.1:n.8632+53_8632+54insC
ENST00000380152.7:c.8632+53_8632+54insC	ENSP00000369497.3:n.8632+53_8632+54insC
ENST00000528762.1:c.130+53_130+54insC	ENSP00000433168.1:n.130+53_130+54insC
ENST00000544455.5:c.8632+53_8632+54insC	ENSP00000439902.1:n.8632+53_8632+54insC
NM_000059.3:c.8632+53_8632+54insC , LRG_293t1:c.8632+53_8632+54insC	NP_000050.2:n.8632+53_8632+54insC
XM_011535203.1:c.8632+53_8632+54insC	XP_011533505.1:n.8632+53_8632+54insC
XM_011535204.1:c.8536+53_8536+54insC	XP_011533506.1:n.8536+53_8536+54insC
XM_011535205.1:c.8632+53_8632+54insC	XP_011533507.1:n.8632+53_8632+54insC
NM_000059.4:c.8632+53_8632+54insC MANE Select	NP_000050.3:n.8632+53_8632+54insC