Canonical Allele Identifier: CA483440156

Gene: BRCA2

Linked Data

• MyVariant Identifiers: chr13:g.32972481G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398344G>T , CM000675.2:g.32398344G>T	GRCh38
NC_000013.10:g.32972481G>T , CM000675.1:g.32972481G>T	GRCh37
NC_000013.9:g.31870481G>T	NCBI36
NG_012772.3:g.87865G>T , LRG_293:g.87865G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*354G>T	ENSP00000434898.2:n.*354G>T
ENST00000528762.2:c.*1198G>T	ENSP00000433168.2:n.*1198G>T
ENST00000530893.7:c.9462G>T	ENSP00000499438.2:p.Leu3154=
ENST00000665585.2:c.*1393G>T	ENSP00000499570.2:n.*1393G>T
ENST00000700202.2:c.9780G>T	ENSP00000514856.2:p.Leu3260=
ENST00000700202.1:c.2247G>T	ENSP00000514856.1:p.Leu749=
ENST00000700203.1:n.1958G>T
ENST00000380152.8:c.9831G>T MANE Select	ENSP00000369497.3:p.Leu3277=
ENST00000544455.6:c.9831G>T	ENSP00000439902.1:p.Leu3277=
ENST00000614259.2:c.9839G>T	ENSP00000506251.1:n.9839G>T
ENST00000680887.1:c.9831G>T	ENSP00000505508.1:p.Leu3277=
ENST00000380152.7:c.9831G>T	ENSP00000369497.3:p.Leu3277=
ENST00000533776.1:n.419G>T
ENST00000544455.5:c.9831G>T	ENSP00000439902.1:p.Leu3277=
NM_000059.3:c.9831G>T , LRG_293t1:c.9831G>T	NP_000050.2:p.Leu3277=
XM_011535203.1:c.9831G>T	XP_011533505.1:p.Leu3277=
XM_011535204.1:c.9735G>T	XP_011533506.1:p.Leu3245=
NM_000059.4:c.9831G>T MANE Select	NP_000050.3:p.Leu3277=