Canonical Allele Identifier: CA2622601720

Gene: BRCA2

Linked Data

• gnomAD v4: 13-32376941-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32376943del , CM000675.2:g.32376943del	GRCh38
NC_000013.10:g.32951080del , CM000675.1:g.32951080del	GRCh37
NC_000013.9:g.31849080del	NCBI36
NG_012772.3:g.66464del , LRG_293:g.66464del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8754+152del	ENSP00000434898.2:n.8754+152del
ENST00000528762.2:c.*121+152del	ENSP00000433168.2:n.*121+152del
ENST00000530893.7:c.8385+152del	ENSP00000499438.2:n.8385+152del
ENST00000665585.2:c.*316+152del	ENSP00000499570.2:n.*316+152del
ENST00000666593.2:c.8754+152del	ENSP00000499256.2:n.8754+152del
ENST00000700202.2:c.8754+152del	ENSP00000514856.2:n.8754+152del
ENST00000700202.1:c.1221+152del	ENSP00000514856.1:n.1221+152del
ENST00000700203.1:n.881+152del
ENST00000380152.8:c.8754+152del MANE Select	ENSP00000369497.3:n.8754+152del
ENST00000544455.6:c.8754+152del	ENSP00000439902.1:n.8754+152del
ENST00000614259.2:c.8762+152del	ENSP00000506251.1:n.8762+152del
ENST00000665585.1:c.1632+152del
ENST00000680887.1:c.8754+152del	ENSP00000505508.1:n.8754+152del
ENST00000380152.7:c.8754+152del	ENSP00000369497.3:n.8754+152del
ENST00000528762.1:c.316+152del	ENSP00000433168.1:n.316+152del
ENST00000544455.5:c.8754+152del	ENSP00000439902.1:n.8754+152del
NM_000059.3:c.8754+152del , LRG_293t1:c.8754+152del	NP_000050.2:n.8754+152del
XM_011535203.1:c.8754+152del	XP_011533505.1:n.8754+152del
XM_011535204.1:c.8658+152del	XP_011533506.1:n.8658+152del
XM_011535205.1:c.8754+152del	XP_011533507.1:n.8754+152del
NM_000059.4:c.8754+152del MANE Select	NP_000050.3:n.8754+152del