Canonical Allele Identifier: CA387754760

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 1705070
• ClinVar RCV Id: RCV002283395
• dbSNP Id: rs1555288153
• MyVariant Identifiers: chr13:g.32950852A>T (hg19) ; chr13:g.32376715A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32376715A>T , CM000675.2:g.32376715A>T	GRCh38
NC_000013.10:g.32950852A>T , CM000675.1:g.32950852A>T	GRCh37
NC_000013.9:g.31848852A>T	NCBI36
NG_012772.3:g.66236A>T , LRG_293:g.66236A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8678A>T	ENSP00000434898.2:p.Gln2893Leu
ENST00000528762.2:c.*45A>T	ENSP00000433168.2:n.*45A>T
ENST00000530893.7:c.8309A>T	ENSP00000499438.2:p.Gln2770Leu
ENST00000665585.2:c.*240A>T	ENSP00000499570.2:n.*240A>T
ENST00000666593.2:c.8678A>T	ENSP00000499256.2:p.Gln2893Leu
ENST00000700202.2:c.8678A>T	ENSP00000514856.2:p.Gln2893Leu
ENST00000700202.1:c.1145A>T	ENSP00000514856.1:p.Gln382Leu
ENST00000700203.1:n.805A>T
ENST00000380152.8:c.8678A>T MANE Select	ENSP00000369497.3:p.Gln2893Leu
ENST00000544455.6:c.8678A>T	ENSP00000439902.1:p.Gln2893Leu
ENST00000614259.2:c.8686A>T	ENSP00000506251.1:n.8686A>T
ENST00000665585.1:c.1556A>T
ENST00000680887.1:c.8678A>T	ENSP00000505508.1:p.Gln2893Leu
ENST00000380152.7:c.8678A>T	ENSP00000369497.3:p.Gln2893Leu
ENST00000528762.1:c.240A>T	ENSP00000433168.1:n.240A>T
ENST00000544455.5:c.8678A>T	ENSP00000439902.1:p.Gln2893Leu
NM_000059.3:c.8678A>T , LRG_293t1:c.8678A>T	NP_000050.2:p.Gln2893Leu
XM_011535203.1:c.8678A>T	XP_011533505.1:p.Gln2893Leu
XM_011535204.1:c.8582A>T	XP_011533506.1:p.Gln2861Leu
XM_011535205.1:c.8678A>T	XP_011533507.1:p.Gln2893Leu
NM_000059.4:c.8678A>T MANE Select	NP_000050.3:p.Gln2893Leu