Canonical Allele Identifier: CA609453891

Gene: BRCA2

Linked Data

• dbSNP Id: rs1277469664
• gnomAD v2: 13-32937235-TCA-T
• gnomAD v3: 13-32363098-TCA-T
• gnomAD v4: 13-32363098-TCA-T
• MyVariant Identifiers: chr13:g.32937236_32937237del (hg19) ; chr13:g.32363099_32363100del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32363099_32363100del , CM000675.2:g.32363099_32363100del	GRCh38
NC_000013.10:g.32937236_32937237del , CM000675.1:g.32937236_32937237del	GRCh37
NC_000013.9:g.31835236_31835237del	NCBI36
NG_012772.3:g.52620_52621del , LRG_293:g.52620_52621del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7977-80_7977-79del	ENSP00000434898.2:n.7977-80_7977-79del
ENST00000528762.2:c.7977-80_7977-79del	ENSP00000433168.2:n.7977-80_7977-79del
ENST00000530893.7:c.7608-80_7608-79del	ENSP00000499438.2:n.7608-80_7608-79del
ENST00000665585.2:c.7977-80_7977-79del	ENSP00000499570.2:n.7977-80_7977-79del
ENST00000666593.2:c.7977-80_7977-79del	ENSP00000499256.2:n.7977-80_7977-79del
ENST00000700202.2:c.7977-80_7977-79del	ENSP00000514856.2:n.7977-80_7977-79del
ENST00000700202.1:c.444-80_444-79del	ENSP00000514856.1:n.444-80_444-79del
ENST00000380152.8:c.7977-80_7977-79del MANE Select	ENSP00000369497.3:n.7977-80_7977-79del
ENST00000544455.6:c.7977-80_7977-79del	ENSP00000439902.1:n.7977-80_7977-79del
ENST00000614259.2:c.7985-80_7985-79del	ENSP00000506251.1:n.7985-80_7985-79del
ENST00000665585.1:c.542-80_542-79del
ENST00000680887.1:c.7977-80_7977-79del	ENSP00000505508.1:n.7977-80_7977-79del
ENST00000380152.7:c.7977-80_7977-79del	ENSP00000369497.3:n.7977-80_7977-79del
ENST00000544455.5:c.7977-80_7977-79del	ENSP00000439902.1:n.7977-80_7977-79del
NM_000059.3:c.7977-80_7977-79del , LRG_293t1:c.7977-80_7977-79del	NP_000050.2:n.7977-80_7977-79del
XM_011535203.1:c.7977-80_7977-79del	XP_011533505.1:n.7977-80_7977-79del
XM_011535204.1:c.7881-80_7881-79del	XP_011533506.1:n.7881-80_7881-79del
XM_011535205.1:c.7977-80_7977-79del	XP_011533507.1:n.7977-80_7977-79del
NM_000059.4:c.7977-80_7977-79del MANE Select	NP_000050.3:n.7977-80_7977-79del