Canonical Allele Identifier: CA6941237

Gene: BRCA2

Linked Data

• ExAC: 13:32944720 ATATATTTCTTTCTTTTGATACAATTAATTTGTTTGTTTGTTTGAGATGGAGTTT / A
• MyVariant Identifiers: chr13:g.32944721_32944774del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32370584_32370637del , CM000675.2:g.32370584_32370637del	GRCh38
NC_000013.10:g.32944721_32944774del , CM000675.1:g.32944721_32944774del	GRCh37
NC_000013.9:g.31842721_31842774del	NCBI36
NG_012772.3:g.60105_60158del , LRG_293:g.60105_60158del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8487+27_8487+80del	ENSP00000434898.2:n.8487+27_8487+80del
ENST00000528762.2:c.8487+27_8487+80del	ENSP00000433168.2:n.8487+27_8487+80del
ENST00000530893.7:c.8118+27_8118+80del	ENSP00000499438.2:n.8118+27_8118+80del
ENST00000665585.2:c.8487+27_8487+80del	ENSP00000499570.2:n.8487+27_8487+80del
ENST00000666593.2:c.8487+27_8487+80del	ENSP00000499256.2:n.8487+27_8487+80del
ENST00000700202.2:c.8487+27_8487+80del	ENSP00000514856.2:n.8487+27_8487+80del
ENST00000700202.1:c.954+27_954+80del	ENSP00000514856.1:n.954+27_954+80del
ENST00000380152.8:c.8487+27_8487+80del MANE Select	ENSP00000369497.3:n.8487+27_8487+80del
ENST00000544455.6:c.8487+27_8487+80del	ENSP00000439902.1:n.8487+27_8487+80del
ENST00000614259.2:c.8495+27_8495+80del	ENSP00000506251.1:n.8495+27_8495+80del
ENST00000665585.1:c.1052+27_1052+80del
ENST00000680887.1:c.8487+27_8487+80del	ENSP00000505508.1:n.8487+27_8487+80del
ENST00000380152.7:c.8487+27_8487+80del	ENSP00000369497.3:n.8487+27_8487+80del
ENST00000544455.5:c.8487+27_8487+80del	ENSP00000439902.1:n.8487+27_8487+80del
NM_000059.3:c.8487+27_8487+80del , LRG_293t1:c.8487+27_8487+80del	NP_000050.2:n.8487+27_8487+80del
XM_011535203.1:c.8487+27_8487+80del	XP_011533505.1:n.8487+27_8487+80del
XM_011535204.1:c.8391+27_8391+80del	XP_011533506.1:n.8391+27_8391+80del
XM_011535205.1:c.8487+27_8487+80del	XP_011533507.1:n.8487+27_8487+80del
NM_000059.4:c.8487+27_8487+80del MANE Select	NP_000050.3:n.8487+27_8487+80del