Canonical Allele Identifier: CA387762844

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32396902T>C , CM000675.2:g.32396902T>C	GRCh38
NC_000013.10:g.32971039T>C , CM000675.1:g.32971039T>C	GRCh37
NC_000013.9:g.31869039T>C	NCBI36
NG_012772.3:g.86423T>C , LRG_293:g.86423T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000059.4:c.9506T>C MANE Select	NP_000050.3:p.Ile3169Thr
ENST00000380152.8:c.9506T>C MANE Select	ENSP00000369497.3:p.Ile3169Thr
NM_000059.3:c.9506T>C , LRG_293t1:c.9506T>C	NP_000050.2:p.Ile3169Thr
ENST00000380152.7:c.9506T>C	ENSP00000369497.3:p.Ile3169Thr
ENST00000470094.1:c.589T>C
ENST00000470094.2:c.*29T>C	ENSP00000434898.2:n.*29T>C
ENST00000528762.2:c.*873T>C	ENSP00000433168.2:n.*873T>C
ENST00000530893.7:c.9137T>C	ENSP00000499438.2:p.Ile3046Thr
ENST00000533776.1:n.94T>C
ENST00000544455.5:c.9506T>C	ENSP00000439902.1:p.Ile3169Thr
ENST00000544455.6:c.9506T>C	ENSP00000439902.1:p.Ile3169Thr
ENST00000614259.2:c.9514T>C	ENSP00000506251.1:n.9514T>C
ENST00000665585.1:c.2384T>C
ENST00000665585.2:c.*1068T>C	ENSP00000499570.2:n.*1068T>C
ENST00000680887.1:c.9506T>C	ENSP00000505508.1:p.Ile3169Thr
ENST00000700202.1:c.1922T>C	ENSP00000514856.1:p.Ile641Thr
ENST00000700202.2:c.9455T>C	ENSP00000514856.2:p.Ile3152Thr
ENST00000700203.1:n.1633T>C
XM_011535203.1:c.9506T>C	XP_011533505.1:p.Ile3169Thr
XM_011535204.1:c.9410T>C	XP_011533506.1:p.Ile3137Thr