Canonical Allele Identifier: CA2082822079

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32394707_32394708delinsAT , CM000675.2:g.32394707_32394708delinsAT	GRCh38
NC_000013.10:g.32968844_32968845delinsAT , CM000675.1:g.32968844_32968845delinsAT	GRCh37
NC_000013.9:g.31866844_31866845delinsAT	NCBI36
NG_012772.3:g.84228_84229delinsAT , LRG_293:g.84228_84229delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.9275_9276delinsAT	ENSP00000434898.2:p.Tyr3092=
ENST00000528762.2:c.*642_*643delinsAT	ENSP00000433168.2:n.*642_*643delinsAT
ENST00000530893.7:c.8906_8907delinsAT	ENSP00000499438.2:p.Tyr2969=
ENST00000665585.2:c.*837_*838delinsAT	ENSP00000499570.2:n.*837_*838delinsAT
ENST00000666593.2:c.*120_*121delinsAT	ENSP00000499256.2:n.*120_*121delinsAT
ENST00000700202.2:c.9224_9225delinsAT	ENSP00000514856.2:p.Tyr3075=
ENST00000700202.1:c.1691_1692delinsAT	ENSP00000514856.1:p.Tyr564=
ENST00000700203.1:n.1402_1403delinsAT
ENST00000380152.8:c.9275_9276delinsAT MANE Select	ENSP00000369497.3:p.Tyr3092=
ENST00000544455.6:c.9275_9276delinsAT	ENSP00000439902.1:p.Tyr3092=
ENST00000614259.2:c.9283_9284delinsAT	ENSP00000506251.1:n.9283_9284delinsAT
ENST00000665585.1:c.2153_2154delinsAT
ENST00000666593.1:c.297_298delinsAT	ENSP00000499256.1:n.297_298delinsAT
ENST00000680887.1:c.9275_9276delinsAT	ENSP00000505508.1:p.Tyr3092=
ENST00000380152.7:c.9275_9276delinsAT	ENSP00000369497.3:p.Tyr3092=
ENST00000470094.1:c.232_233delinsAT
ENST00000544455.5:c.9275_9276delinsAT	ENSP00000439902.1:p.Tyr3092=
NM_000059.3:c.9275_9276delinsAT , LRG_293t1:c.9275_9276delinsAT	NP_000050.2:p.Tyr3092=
XM_011535203.1:c.9275_9276delinsAT	XP_011533505.1:p.Tyr3092=
XM_011535204.1:c.9179_9180delinsAT	XP_011533506.1:p.Tyr3060=
NM_000059.4:c.9275_9276delinsAT MANE Select	NP_000050.3:p.Tyr3092=