Canonical Allele Identifier: CA387765957

Gene: BRCA2

Linked Data

• MyVariant Identifiers: chr13:g.32972436A>C (hg19) ; chr13:g.32398299A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398299A>C , CM000675.2:g.32398299A>C	GRCh38
NC_000013.10:g.32972436A>C , CM000675.1:g.32972436A>C	GRCh37
NC_000013.9:g.31870436A>C	NCBI36
NG_012772.3:g.87820A>C , LRG_293:g.87820A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.*309A>C	ENSP00000434898.2:n.*309A>C
ENST00000528762.2:c.*1153A>C	ENSP00000433168.2:n.*1153A>C
ENST00000530893.7:c.9417A>C	ENSP00000499438.2:p.Gln3139His
ENST00000665585.2:c.*1348A>C	ENSP00000499570.2:n.*1348A>C
ENST00000700202.2:c.9735A>C	ENSP00000514856.2:p.Gln3245His
ENST00000700202.1:c.2202A>C	ENSP00000514856.1:p.Gln734His
ENST00000700203.1:n.1913A>C
ENST00000380152.8:c.9786A>C MANE Select	ENSP00000369497.3:p.Gln3262His
ENST00000544455.6:c.9786A>C	ENSP00000439902.1:p.Gln3262His
ENST00000614259.2:c.9794A>C	ENSP00000506251.1:n.9794A>C
ENST00000680887.1:c.9786A>C	ENSP00000505508.1:p.Gln3262His
ENST00000380152.7:c.9786A>C	ENSP00000369497.3:p.Gln3262His
ENST00000533776.1:n.374A>C
ENST00000544455.5:c.9786A>C	ENSP00000439902.1:p.Gln3262His
NM_000059.3:c.9786A>C , LRG_293t1:c.9786A>C	NP_000050.2:p.Gln3262His
XM_011535203.1:c.9786A>C	XP_011533505.1:p.Gln3262His
XM_011535204.1:c.9690A>C	XP_011533506.1:p.Gln3230His
NM_000059.4:c.9786A>C MANE Select	NP_000050.3:p.Gln3262His