Canonical Allele Identifier: CA387760852

Gene: BRCA2

Linked Data

• MyVariant Identifiers: chr13:g.32968861T>A (hg19) ; chr13:g.32394724T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32394724T>A , CM000675.2:g.32394724T>A	GRCh38
NC_000013.10:g.32968861T>A , CM000675.1:g.32968861T>A	GRCh37
NC_000013.9:g.31866861T>A	NCBI36
NG_012772.3:g.84245T>A , LRG_293:g.84245T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.9292T>A	ENSP00000434898.2:p.Tyr3098Asn
ENST00000528762.2:c.*659T>A	ENSP00000433168.2:n.*659T>A
ENST00000530893.7:c.8923T>A	ENSP00000499438.2:p.Tyr2975Asn
ENST00000665585.2:c.*854T>A	ENSP00000499570.2:n.*854T>A
ENST00000666593.2:c.*137T>A	ENSP00000499256.2:n.*137T>A
ENST00000700202.2:c.9241T>A	ENSP00000514856.2:p.Tyr3081Asn
ENST00000700202.1:c.1708T>A	ENSP00000514856.1:p.Tyr570Asn
ENST00000700203.1:n.1419T>A
ENST00000380152.8:c.9292T>A MANE Select	ENSP00000369497.3:p.Tyr3098Asn
ENST00000544455.6:c.9292T>A	ENSP00000439902.1:p.Tyr3098Asn
ENST00000614259.2:c.9300T>A	ENSP00000506251.1:n.9300T>A
ENST00000665585.1:c.2170T>A
ENST00000666593.1:c.314T>A	ENSP00000499256.1:n.314T>A
ENST00000680887.1:c.9292T>A	ENSP00000505508.1:p.Tyr3098Asn
ENST00000380152.7:c.9292T>A	ENSP00000369497.3:p.Tyr3098Asn
ENST00000470094.1:c.249T>A
ENST00000544455.5:c.9292T>A	ENSP00000439902.1:p.Tyr3098Asn
NM_000059.3:c.9292T>A , LRG_293t1:c.9292T>A	NP_000050.2:p.Tyr3098Asn
XM_011535203.1:c.9292T>A	XP_011533505.1:p.Tyr3098Asn
XM_011535204.1:c.9196T>A	XP_011533506.1:p.Tyr3066Asn
NM_000059.4:c.9292T>A MANE Select	NP_000050.3:p.Tyr3098Asn