Canonical Allele Identifier: CA10579834

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32394929T>C , CM000675.2:g.32394929T>C	GRCh38
NC_000013.10:g.32969066T>C , CM000675.1:g.32969066T>C	GRCh37
NC_000013.9:g.31867066T>C	NCBI36
NG_012772.3:g.84450T>C , LRG_293:g.84450T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000059.4:c.9497T>C MANE Select	NP_000050.3:p.Val3166Ala
ENST00000380152.8:c.9497T>C MANE Select	ENSP00000369497.3:p.Val3166Ala
NM_000059.3:c.9497T>C , LRG_293t1:c.9497T>C	NP_000050.2:p.Val3166Ala
ENST00000380152.7:c.9497T>C	ENSP00000369497.3:p.Val3166Ala
ENST00000470094.1:c.454T>C
ENST00000470094.2:c.9497T>C	ENSP00000434898.2:p.Val3166Ala
ENST00000528762.2:c.*864T>C	ENSP00000433168.2:n.*864T>C
ENST00000530893.7:c.9128T>C	ENSP00000499438.2:p.Val3043Ala
ENST00000544455.5:c.9497T>C	ENSP00000439902.1:p.Val3166Ala
ENST00000544455.6:c.9497T>C	ENSP00000439902.1:p.Val3166Ala
ENST00000614259.2:c.9505T>C	ENSP00000506251.1:n.9505T>C
ENST00000665585.1:c.2375T>C
ENST00000665585.2:c.*1059T>C	ENSP00000499570.2:n.*1059T>C
ENST00000666593.1:c.519T>C	ENSP00000499256.1:n.519T>C
ENST00000666593.2:c.*342T>C	ENSP00000499256.2:n.*342T>C
ENST00000680887.1:c.9497T>C	ENSP00000505508.1:p.Val3166Ala
ENST00000700202.1:c.1913T>C	ENSP00000514856.1:p.Val638Ala
ENST00000700202.2:c.9446T>C	ENSP00000514856.2:p.Val3149Ala
ENST00000700203.1:n.1624T>C
XM_011535203.1:c.9497T>C	XP_011533505.1:p.Val3166Ala
XM_011535204.1:c.9401T>C	XP_011533506.1:p.Val3134Ala