Canonical Allele Identifier: CA387757307

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 986954
• ClinVar RCV Id: RCV001268139 ; RCV003462846 ; RCV003770399
• dbSNP Id: rs2072903033
• MyVariant Identifiers: chr13:g.32953634A>T (hg19) ; chr13:g.32379497A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32379497A>T , CM000675.2:g.32379497A>T	GRCh38
NC_000013.10:g.32953634A>T , CM000675.1:g.32953634A>T	GRCh37
NC_000013.9:g.31851634A>T	NCBI36
NG_012772.3:g.69018A>T , LRG_293:g.69018A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8935A>T	ENSP00000434898.2:p.Lys2979Ter
ENST00000528762.2:c.*302A>T	ENSP00000433168.2:n.*302A>T
ENST00000530893.7:c.8566A>T	ENSP00000499438.2:p.Lys2856Ter
ENST00000665585.2:c.*497A>T	ENSP00000499570.2:n.*497A>T
ENST00000666593.2:c.8935A>T	ENSP00000499256.2:p.Lys2979Ter
ENST00000700202.2:c.8935A>T	ENSP00000514856.2:p.Lys2979Ter
ENST00000700202.1:c.1402A>T	ENSP00000514856.1:p.Lys468Ter
ENST00000700203.1:n.1062A>T
ENST00000380152.8:c.8935A>T MANE Select	ENSP00000369497.3:p.Lys2979Ter
ENST00000544455.6:c.8935A>T	ENSP00000439902.1:p.Lys2979Ter
ENST00000614259.2:c.8943A>T	ENSP00000506251.1:n.8943A>T
ENST00000665585.1:c.1813A>T
ENST00000680887.1:c.8935A>T	ENSP00000505508.1:p.Lys2979Ter
ENST00000380152.7:c.8935A>T	ENSP00000369497.3:p.Lys2979Ter
ENST00000544455.5:c.8935A>T	ENSP00000439902.1:p.Lys2979Ter
NM_000059.3:c.8935A>T , LRG_293t1:c.8935A>T	NP_000050.2:p.Lys2979Ter
XM_011535203.1:c.8935A>T	XP_011533505.1:p.Lys2979Ter
XM_011535204.1:c.8839A>T	XP_011533506.1:p.Lys2947Ter
XM_011535205.1:c.8755-253A>T	XP_011533507.1:n.8755-253A>T
NM_000059.4:c.8935A>T MANE Select	NP_000050.3:p.Lys2979Ter