Canonical Allele Identifier: CA1139771309

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32362680_32362691del , CM000675.2:g.32362680_32362691del	GRCh38
NC_000013.10:g.32936817_32936828del , CM000675.1:g.32936817_32936828del	GRCh37
NC_000013.9:g.31834817_31834828del	NCBI36
NG_012772.3:g.52201_52212del , LRG_293:g.52201_52212del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7963_7974del	ENSP00000434898.2:p.Gln2655_Tyr2658del
ENST00000528762.2:c.7963_7974del	ENSP00000433168.2:p.Gln2655_Tyr2658del
ENST00000530893.7:c.7594_7605del	ENSP00000499438.2:p.Gln2532_Tyr2535del
ENST00000665585.2:c.7963_7974del	ENSP00000499570.2:p.Gln2655_Tyr2658del
ENST00000666593.2:c.7963_7974del	ENSP00000499256.2:p.Gln2655_Tyr2658del
ENST00000700202.2:c.7963_7974del	ENSP00000514856.2:p.Gln2655_Tyr2658del
ENST00000700202.1:c.430_441del	ENSP00000514856.1:p.Gln144_Tyr147del
ENST00000380152.8:c.7963_7974del MANE Select	ENSP00000369497.3:p.Gln2655_Tyr2658del
ENST00000544455.6:c.7963_7974del	ENSP00000439902.1:p.Gln2655_Tyr2658del
ENST00000614259.2:c.7971_7982del	ENSP00000506251.1:n.7971_7982del
ENST00000665585.1:c.528_539del
ENST00000680887.1:c.7963_7974del	ENSP00000505508.1:p.Gln2655_Tyr2658del
ENST00000380152.7:c.7963_7974del	ENSP00000369497.3:p.Gln2655_Tyr2658del
ENST00000544455.5:c.7963_7974del	ENSP00000439902.1:p.Gln2655_Tyr2658del
NM_000059.3:c.7963_7974del , LRG_293t1:c.7963_7974del	NP_000050.2:p.Gln2655_Tyr2658del
XM_011535203.1:c.7963_7974del	XP_011533505.1:p.Gln2655_Tyr2658del
XM_011535204.1:c.7867_7878del	XP_011533506.1:p.Gln2623_Tyr2626del
XM_011535205.1:c.7963_7974del	XP_011533507.1:p.Gln2655_Tyr2658del
NM_000059.4:c.7963_7974del MANE Select	NP_000050.3:p.Gln2655_Tyr2658del