Canonical Allele Identifier: CA387757994

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32380058T>C , CM000675.2:g.32380058T>C	GRCh38
NC_000013.10:g.32954195T>C , CM000675.1:g.32954195T>C	GRCh37
NC_000013.9:g.31852195T>C	NCBI36
NG_012772.3:g.69579T>C , LRG_293:g.69579T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000059.4:c.9169T>C MANE Select	NP_000050.3:p.Phe3057Leu
ENST00000380152.8:c.9169T>C MANE Select	ENSP00000369497.3:p.Phe3057Leu
NM_000059.3:c.9169T>C , LRG_293t1:c.9169T>C	NP_000050.2:p.Phe3057Leu
ENST00000380152.7:c.9169T>C	ENSP00000369497.3:p.Phe3057Leu
ENST00000470094.1:c.126T>C
ENST00000470094.2:c.9169T>C	ENSP00000434898.2:p.Phe3057Leu
ENST00000528762.2:c.*536T>C	ENSP00000433168.2:n.*536T>C
ENST00000530893.7:c.8800T>C	ENSP00000499438.2:p.Phe2934Leu
ENST00000544455.5:c.9169T>C	ENSP00000439902.1:p.Phe3057Leu
ENST00000544455.6:c.9169T>C	ENSP00000439902.1:p.Phe3057Leu
ENST00000614259.2:c.9177T>C	ENSP00000506251.1:n.9177T>C
ENST00000665585.1:c.2047T>C
ENST00000665585.2:c.*731T>C	ENSP00000499570.2:n.*731T>C
ENST00000666593.1:c.52T>C	ENSP00000499256.1:p.Phe18Leu
ENST00000666593.2:c.9169T>C	ENSP00000499256.2:p.Phe3057Leu
ENST00000680887.1:c.9169T>C	ENSP00000505508.1:p.Phe3057Leu
ENST00000700202.1:c.1585T>C	ENSP00000514856.1:p.Phe529Leu
ENST00000700202.2:c.9118T>C	ENSP00000514856.2:p.Phe3040Leu
ENST00000700203.1:n.1296T>C
XM_011535203.1:c.9169T>C	XP_011533505.1:p.Phe3057Leu
XM_011535204.1:c.9073T>C	XP_011533506.1:p.Phe3025Leu