Canonical Allele Identifier: CA2622601575

Gene: BRCA2

Linked Data

• gnomAD v4: 13-32376531-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32376531_32376532insG , CM000675.2:g.32376531_32376532insG	GRCh38
NC_000013.10:g.32950668_32950669insG , CM000675.1:g.32950668_32950669insG	GRCh37
NC_000013.9:g.31848668_31848669insG	NCBI36
NG_012772.3:g.66052_66053insG , LRG_293:g.66052_66053insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8633-139_8633-138insG	ENSP00000434898.2:n.8633-139_8633-138insG
ENST00000528762.2:c.8697-139_8697-138insG	ENSP00000433168.2:n.8697-139_8697-138insG
ENST00000530893.7:c.8264-139_8264-138insG	ENSP00000499438.2:n.8264-139_8264-138insG
ENST00000665585.2:c.*195-139_*195-138insG	ENSP00000499570.2:n.*195-139_*195-138insG
ENST00000666593.2:c.8633-139_8633-138insG	ENSP00000499256.2:n.8633-139_8633-138insG
ENST00000700202.2:c.8633-139_8633-138insG	ENSP00000514856.2:n.8633-139_8633-138insG
ENST00000700202.1:c.1100-139_1100-138insG	ENSP00000514856.1:n.1100-139_1100-138insG
ENST00000700203.1:n.621_622insG
ENST00000380152.8:c.8633-139_8633-138insG MANE Select	ENSP00000369497.3:n.8633-139_8633-138insG
ENST00000544455.6:c.8633-139_8633-138insG	ENSP00000439902.1:n.8633-139_8633-138insG
ENST00000614259.2:c.8641-139_8641-138insG	ENSP00000506251.1:n.8641-139_8641-138insG
ENST00000665585.1:c.1511-139_1511-138insG
ENST00000680887.1:c.8633-139_8633-138insG	ENSP00000505508.1:n.8633-139_8633-138insG
ENST00000380152.7:c.8633-139_8633-138insG	ENSP00000369497.3:n.8633-139_8633-138insG
ENST00000528762.1:c.195-139_195-138insG	ENSP00000433168.1:n.195-139_195-138insG
ENST00000544455.5:c.8633-139_8633-138insG	ENSP00000439902.1:n.8633-139_8633-138insG
NM_000059.3:c.8633-139_8633-138insG , LRG_293t1:c.8633-139_8633-138insG	NP_000050.2:n.8633-139_8633-138insG
XM_011535203.1:c.8633-139_8633-138insG	XP_011533505.1:n.8633-139_8633-138insG
XM_011535204.1:c.8537-139_8537-138insG	XP_011533506.1:n.8537-139_8537-138insG
XM_011535205.1:c.8633-139_8633-138insG	XP_011533507.1:n.8633-139_8633-138insG
NM_000059.4:c.8633-139_8633-138insG MANE Select	NP_000050.3:n.8633-139_8633-138insG