Canonical Allele Identifier: CA387767533

Gene: BRCA2

Linked Data

• MyVariant Identifiers: chr13:g.32972629A>C (hg19) ; chr13:g.32398492A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398492A>C , CM000675.2:g.32398492A>C	GRCh38
NC_000013.10:g.32972629A>C , CM000675.1:g.32972629A>C	GRCh37
NC_000013.9:g.31870629A>C	NCBI36
NG_012772.3:g.88013A>C , LRG_293:g.88013A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.*502A>C	ENSP00000434898.2:n.*502A>C
ENST00000528762.2:c.*1346A>C	ENSP00000433168.2:n.*1346A>C
ENST00000530893.7:c.9610A>C	ENSP00000499438.2:p.Lys3204Gln
ENST00000665585.2:c.*1541A>C	ENSP00000499570.2:n.*1541A>C
ENST00000700202.2:c.9928A>C	ENSP00000514856.2:p.Lys3310Gln
ENST00000700202.1:c.2395A>C	ENSP00000514856.1:p.Lys799Gln
ENST00000700203.1:n.2106A>C
ENST00000380152.8:c.9979A>C MANE Select	ENSP00000369497.3:p.Lys3327Gln
ENST00000544455.6:c.9979A>C	ENSP00000439902.1:p.Lys3327Gln
ENST00000614259.2:c.9987A>C	ENSP00000506251.1:n.9987A>C
ENST00000680887.1:c.9979A>C	ENSP00000505508.1:p.Lys3327Gln
ENST00000380152.7:c.9979A>C	ENSP00000369497.3:p.Lys3327Gln
ENST00000544455.5:c.9979A>C	ENSP00000439902.1:p.Lys3327Gln
NM_000059.3:c.9979A>C , LRG_293t1:c.9979A>C	NP_000050.2:p.Lys3327Gln
XM_011535203.1:c.9979A>C	XP_011533505.1:p.Lys3327Gln
XM_011535204.1:c.9883A>C	XP_011533506.1:p.Lys3295Gln
NM_000059.4:c.9979A>C MANE Select	NP_000050.3:p.Lys3327Gln