Canonical Allele Identifier: CA387747139

Gene: BRCA2

Linked Data

• dbSNP Id: rs431825359
• MyVariant Identifiers: chr13:g.32936751G>C (hg19) ; chr13:g.32362614G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32362614G>C , CM000675.2:g.32362614G>C	GRCh38
NC_000013.10:g.32936751G>C , CM000675.1:g.32936751G>C	GRCh37
NC_000013.9:g.31834751G>C	NCBI36
NG_012772.3:g.52135G>C , LRG_293:g.52135G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7897G>C	ENSP00000434898.2:p.Ala2633Pro
ENST00000528762.2:c.7897G>C	ENSP00000433168.2:p.Ala2633Pro
ENST00000530893.7:c.7528G>C	ENSP00000499438.2:p.Ala2510Pro
ENST00000665585.2:c.7897G>C	ENSP00000499570.2:p.Ala2633Pro
ENST00000666593.2:c.7897G>C	ENSP00000499256.2:p.Ala2633Pro
ENST00000700202.2:c.7897G>C	ENSP00000514856.2:p.Ala2633Pro
ENST00000700202.1:c.364G>C	ENSP00000514856.1:p.Ala122Pro
ENST00000380152.8:c.7897G>C MANE Select	ENSP00000369497.3:p.Ala2633Pro
ENST00000544455.6:c.7897G>C	ENSP00000439902.1:p.Ala2633Pro
ENST00000614259.2:c.7905G>C	ENSP00000506251.1:p.Gln2635His
ENST00000665585.1:c.462G>C
ENST00000680887.1:c.7897G>C	ENSP00000505508.1:p.Ala2633Pro
ENST00000380152.7:c.7897G>C	ENSP00000369497.3:p.Ala2633Pro
ENST00000544455.5:c.7897G>C	ENSP00000439902.1:p.Ala2633Pro
ENST00000614259.1:n.7905G>C
NM_000059.3:c.7897G>C , LRG_293t1:c.7897G>C	NP_000050.2:p.Ala2633Pro
XM_011535203.1:c.7897G>C	XP_011533505.1:p.Ala2633Pro
XM_011535204.1:c.7801G>C	XP_011533506.1:p.Ala2601Pro
XM_011535205.1:c.7897G>C	XP_011533507.1:p.Ala2633Pro
NM_000059.4:c.7897G>C MANE Select	NP_000050.3:p.Ala2633Pro