Canonical Allele Identifier: CA2622603345

Gene: BRCA2

Linked Data

• gnomAD v4: 13-32399180-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32399180G>A , CM000675.2:g.32399180G>A	GRCh38
NC_000013.10:g.32973317G>A , CM000675.1:g.32973317G>A	GRCh37
NC_000013.9:g.31871317G>A	NCBI36
NG_012772.3:g.88701G>A , LRG_293:g.88701G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.*1190G>A	ENSP00000434898.2:n.*1190G>A
ENST00000530893.7:c.*410G>A	ENSP00000499438.2:n.*410G>A
ENST00000380152.8:c.*410G>A MANE Select	ENSP00000369497.3:n.*410G>A
ENST00000544455.6:c.*410G>A	ENSP00000439902.1:n.*410G>A
ENST00000614259.2:c.10675G>A	ENSP00000506251.1:n.10675G>A
ENST00000680887.1:c.*410G>A	ENSP00000505508.1:n.*410G>A
ENST00000380152.7:c.*410G>A	ENSP00000369497.3:n.*410G>A
ENST00000544455.5:c.*410G>A	ENSP00000439902.1:n.*410G>A
NM_000059.3:c.*410G>A , LRG_293t1:c.*410G>A	NP_000050.2:n.*410G>A
XM_011535203.1:c.*410G>A	XP_011533505.1:n.*410G>A
XM_011535204.1:c.*410G>A	XP_011533506.1:n.*410G>A
NM_000059.4:c.*410G>A MANE Select	NP_000050.3:n.*410G>A