Canonical Allele Identifier: CA019261

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 254529
• ClinVar RCV Id: RCV000241385 ; RCV001384094 ; RCV002356339
• dbSNP Id: rs80359417
• MyVariant Identifiers: chr13:g.32912449_32912452del (hg19) ; chr13:g.32338312_32338315del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32338312_32338315del , CM000675.2:g.32338312_32338315del	GRCh38
NC_000013.10:g.32912449_32912452del , CM000675.1:g.32912449_32912452del	GRCh37
NC_000013.9:g.31810449_31810452del	NCBI36
NG_012772.3:g.27833_27836del , LRG_293:g.27833_27836del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.3957_3960del	ENSP00000434898.2:p.Asn1319LysfsTer15
ENST00000528762.2:c.3957_3960del	ENSP00000433168.2:p.Asn1319LysfsTer15
ENST00000530893.7:c.3588_3591del	ENSP00000499438.2:p.Asn1196LysfsTer15
ENST00000665585.2:c.3957_3960del	ENSP00000499570.2:p.Asn1319LysfsTer15
ENST00000666593.2:c.3957_3960del	ENSP00000499256.2:p.Asn1319LysfsTer15
ENST00000700202.2:c.3957_3960del	ENSP00000514856.2:p.Asn1319LysfsTer15
ENST00000380152.8:c.3957_3960del MANE Select	ENSP00000369497.3:p.Asn1319LysfsTer15
ENST00000544455.6:c.3957_3960del	ENSP00000439902.1:p.Asn1319LysfsTer15
ENST00000614259.2:c.3957_3960del	ENSP00000506251.1:p.Asn1319LysfsTer15
ENST00000680887.1:c.3957_3960del	ENSP00000505508.1:p.Asn1319LysfsTer15
ENST00000380152.7:c.3957_3960del	ENSP00000369497.3:p.Asn1319LysfsTer15
ENST00000544455.5:c.3957_3960del	ENSP00000439902.1:p.Asn1319LysfsTer15
ENST00000614259.1:n.3957_3960del
NM_000059.3:c.3957_3960del , LRG_293t1:c.3957_3960del	NP_000050.2:p.Asn1319LysfsTer15
XM_011535203.1:c.3957_3960del	XP_011533505.1:p.Asn1319LysfsTer15
XM_011535204.1:c.3957_3960del	XP_011533506.1:p.Asn1319LysfsTer15
XM_011535205.1:c.3957_3960del	XP_011533507.1:p.Asn1319LysfsTer15
NM_000059.4:c.3957_3960del MANE Select	NP_000050.3:p.Asn1319LysfsTer15