Canonical Allele Identifier: CA387765726

Gene: BRCA2

Linked Data

• MyVariant Identifiers: chr13:g.32972407T>G (hg19) ; chr13:g.32398270T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398270T>G , CM000675.2:g.32398270T>G	GRCh38
NC_000013.10:g.32972407T>G , CM000675.1:g.32972407T>G	GRCh37
NC_000013.9:g.31870407T>G	NCBI36
NG_012772.3:g.87791T>G , LRG_293:g.87791T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.*280T>G	ENSP00000434898.2:n.*280T>G
ENST00000528762.2:c.*1124T>G	ENSP00000433168.2:n.*1124T>G
ENST00000530893.7:c.9388T>G	ENSP00000499438.2:p.Cys3130Gly
ENST00000665585.2:c.*1319T>G	ENSP00000499570.2:n.*1319T>G
ENST00000700202.2:c.9706T>G	ENSP00000514856.2:p.Cys3236Gly
ENST00000700202.1:c.2173T>G	ENSP00000514856.1:p.Cys725Gly
ENST00000700203.1:n.1884T>G
ENST00000380152.8:c.9757T>G MANE Select	ENSP00000369497.3:p.Cys3253Gly
ENST00000544455.6:c.9757T>G	ENSP00000439902.1:p.Cys3253Gly
ENST00000614259.2:c.9765T>G	ENSP00000506251.1:n.9765T>G
ENST00000680887.1:c.9757T>G	ENSP00000505508.1:p.Cys3253Gly
ENST00000380152.7:c.9757T>G	ENSP00000369497.3:p.Cys3253Gly
ENST00000470094.1:c.840T>G
ENST00000533776.1:n.345T>G
ENST00000544455.5:c.9757T>G	ENSP00000439902.1:p.Cys3253Gly
NM_000059.3:c.9757T>G , LRG_293t1:c.9757T>G	NP_000050.2:p.Cys3253Gly
XM_011535203.1:c.9757T>G	XP_011533505.1:p.Cys3253Gly
XM_011535204.1:c.9661T>G	XP_011533506.1:p.Cys3221Gly
NM_000059.4:c.9757T>G MANE Select	NP_000050.3:p.Cys3253Gly