Canonical Allele Identifier: CA387747102

Gene: BRCA2

Linked Data

• MyVariant Identifiers: chr13:g.32936731G>C (hg19) ; chr13:g.32362594G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32362594G>C , CM000675.2:g.32362594G>C	GRCh38
NC_000013.10:g.32936731G>C , CM000675.1:g.32936731G>C	GRCh37
NC_000013.9:g.31834731G>C	NCBI36
NG_012772.3:g.52115G>C , LRG_293:g.52115G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7877G>C	ENSP00000434898.2:p.Trp2626Ser
ENST00000528762.2:c.7877G>C	ENSP00000433168.2:p.Trp2626Ser
ENST00000530893.7:c.7508G>C	ENSP00000499438.2:p.Trp2503Ser
ENST00000665585.2:c.7877G>C	ENSP00000499570.2:p.Trp2626Ser
ENST00000666593.2:c.7877G>C	ENSP00000499256.2:p.Trp2626Ser
ENST00000700202.2:c.7877G>C	ENSP00000514856.2:p.Trp2626Ser
ENST00000700202.1:c.344G>C	ENSP00000514856.1:p.Trp115Ser
ENST00000380152.8:c.7877G>C MANE Select	ENSP00000369497.3:p.Trp2626Ser
ENST00000544455.6:c.7877G>C	ENSP00000439902.1:p.Trp2626Ser
ENST00000614259.2:c.7885G>C	ENSP00000506251.1:p.Gly2629Arg
ENST00000665585.1:c.442G>C
ENST00000680887.1:c.7877G>C	ENSP00000505508.1:p.Trp2626Ser
ENST00000380152.7:c.7877G>C	ENSP00000369497.3:p.Trp2626Ser
ENST00000544455.5:c.7877G>C	ENSP00000439902.1:p.Trp2626Ser
ENST00000614259.1:n.7885G>C
NM_000059.3:c.7877G>C , LRG_293t1:c.7877G>C	NP_000050.2:p.Trp2626Ser
XM_011535203.1:c.7877G>C	XP_011533505.1:p.Trp2626Ser
XM_011535204.1:c.7781G>C	XP_011533506.1:p.Trp2594Ser
XM_011535205.1:c.7877G>C	XP_011533507.1:p.Trp2626Ser
NM_000059.4:c.7877G>C MANE Select	NP_000050.3:p.Trp2626Ser