Canonical Allele Identifier: CA609091387

Gene: BRCA2

Linked Data

• dbSNP Id: rs1368217027
• gnomAD v2: 13-32931571-TGAACTTAA-T
• gnomAD v3: 13-32357434-TGAACTTAA-T
• gnomAD v4: 13-32357434-TGAACTTAA-T
• MyVariant Identifiers: chr13:g.32931572_32931579del (hg19) ; chr13:g.32357435_32357442del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32357437_32357444del , CM000675.2:g.32357437_32357444del	GRCh38
NC_000013.10:g.32931574_32931581del , CM000675.1:g.32931574_32931581del	GRCh37
NC_000013.9:g.31829574_31829581del	NCBI36
NG_012772.3:g.46958_46965del , LRG_293:g.46958_46965del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7618-305_7618-298del	ENSP00000434898.2:n.7618-305_7618-298del
ENST00000528762.2:c.7618-305_7618-298del	ENSP00000433168.2:n.7618-305_7618-298del
ENST00000530893.7:c.7249-305_7249-298del	ENSP00000499438.2:n.7249-305_7249-298del
ENST00000665585.2:c.7618-305_7618-298del	ENSP00000499570.2:n.7618-305_7618-298del
ENST00000666593.2:c.7618-305_7618-298del	ENSP00000499256.2:n.7618-305_7618-298del
ENST00000700202.2:c.7618-305_7618-298del	ENSP00000514856.2:n.7618-305_7618-298del
ENST00000700202.1:c.85-305_85-298del	ENSP00000514856.1:n.85-305_85-298del
ENST00000380152.8:c.7618-305_7618-298del MANE Select	ENSP00000369497.3:n.7618-305_7618-298del
ENST00000544455.6:c.7618-305_7618-298del	ENSP00000439902.1:n.7618-305_7618-298del
ENST00000614259.2:c.7618-305_7618-298del	ENSP00000506251.1:n.7618-305_7618-298del
ENST00000665585.1:c.183-305_183-298del
ENST00000680887.1:c.7618-305_7618-298del	ENSP00000505508.1:n.7618-305_7618-298del
ENST00000380152.7:c.7618-305_7618-298del	ENSP00000369497.3:n.7618-305_7618-298del
ENST00000544455.5:c.7618-305_7618-298del	ENSP00000439902.1:n.7618-305_7618-298del
ENST00000614259.1:n.7618-305_7618-298del
NM_000059.3:c.7618-305_7618-298del , LRG_293t1:c.7618-305_7618-298del	NP_000050.2:n.7618-305_7618-298del
XM_011535203.1:c.7618-305_7618-298del	XP_011533505.1:n.7618-305_7618-298del
XM_011535204.1:c.7522-305_7522-298del	XP_011533506.1:n.7522-305_7522-298del
XM_011535205.1:c.7618-305_7618-298del	XP_011533507.1:n.7618-305_7618-298del
NM_000059.4:c.7618-305_7618-298del MANE Select	NP_000050.3:n.7618-305_7618-298del