Canonical Allele Identifier: CA387767929

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 1788982
• ClinVar RCV Id: RCV002446130
• MyVariant Identifiers: chr13:g.32972731C>A (hg19) ; chr13:g.32398594C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398594C>A , CM000675.2:g.32398594C>A	GRCh38
NC_000013.10:g.32972731C>A , CM000675.1:g.32972731C>A	GRCh37
NC_000013.9:g.31870731C>A	NCBI36
NG_012772.3:g.88115C>A , LRG_293:g.88115C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*604C>A	ENSP00000434898.2:n.*604C>A
ENST00000528762.2:c.*1448C>A	ENSP00000433168.2:n.*1448C>A
ENST00000530893.7:c.9712C>A	ENSP00000499438.2:p.Gln3238Lys
ENST00000665585.2:c.*1643C>A	ENSP00000499570.2:n.*1643C>A
ENST00000700202.2:c.10030C>A	ENSP00000514856.2:p.Gln3344Lys
ENST00000700202.1:c.2497C>A	ENSP00000514856.1:p.Gln833Lys
ENST00000700203.1:n.2208C>A
ENST00000380152.8:c.10081C>A MANE Select	ENSP00000369497.3:p.Gln3361Lys
ENST00000544455.6:c.10081C>A	ENSP00000439902.1:p.Gln3361Lys
ENST00000614259.2:c.10089C>A	ENSP00000506251.1:n.10089C>A
ENST00000680887.1:c.10081C>A	ENSP00000505508.1:p.Gln3361Lys
ENST00000380152.7:c.10081C>A	ENSP00000369497.3:p.Gln3361Lys
ENST00000544455.5:c.10081C>A	ENSP00000439902.1:p.Gln3361Lys
NM_000059.3:c.10081C>A , LRG_293t1:c.10081C>A	NP_000050.2:p.Gln3361Lys
XM_011535203.1:c.10081C>A	XP_011533505.1:p.Gln3361Lys
XM_011535204.1:c.9985C>A	XP_011533506.1:p.Gln3329Lys
NM_000059.4:c.10081C>A MANE Select	NP_000050.3:p.Gln3361Lys