Canonical Allele Identifier: CA2541660433

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32371029_32371030insCCTCGTCCTTCT , CM000675.2:g.32371029_32371030insCCTCGTCCTTCT	GRCh38
NC_000013.10:g.32945166_32945167insCCTCGTCCTTCT , CM000675.1:g.32945166_32945167insCCTCGTCCTTCT	GRCh37
NC_000013.9:g.31843166_31843167insCCTCGTCCTTCT	NCBI36
NG_012772.3:g.60550_60551insCCTCGTCCTTCT , LRG_293:g.60550_60551insCCTCGTCCTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8561_8562insCCTCGTCCTTCT	ENSP00000434898.2:p.Tyr2854_Val2855insLeuValLeuLeu
ENST00000528762.2:c.8561_8562insCCTCGTCCTTCT	ENSP00000433168.2:p.Tyr2854_Val2855insLeuValLeuLeu
ENST00000530893.7:c.8192_8193insCCTCGTCCTTCT	ENSP00000499438.2:p.Tyr2731_Val2732insLeuValLeuLeu
ENST00000665585.2:c.8561_8562insCCTCGTCCTTCT	ENSP00000499570.2:p.Tyr2854_Val2855insLeuValLeuLeu
ENST00000666593.2:c.8561_8562insCCTCGTCCTTCT	ENSP00000499256.2:p.Tyr2854_Val2855insLeuValLeuLeu
ENST00000700202.2:c.8561_8562insCCTCGTCCTTCT	ENSP00000514856.2:p.Tyr2854_Val2855insLeuValLeuLeu
ENST00000700202.1:c.1028_1029insCCTCGTCCTTCT	ENSP00000514856.1:p.Tyr343_Val344insLeuValLeuLeu
ENST00000380152.8:c.8561_8562insCCTCGTCCTTCT MANE Select	ENSP00000369497.3:p.Tyr2854_Val2855insLeuValLeuLeu
ENST00000544455.6:c.8561_8562insCCTCGTCCTTCT	ENSP00000439902.1:p.Tyr2854_Val2855insLeuValLeuLeu
ENST00000614259.2:c.8569_8570insCCTCGTCCTTCT	ENSP00000506251.1:n.8569_8570insCCTCGTCCTTCT
ENST00000665585.1:c.1126_1127insCCTCGTCCTTCT
ENST00000680887.1:c.8561_8562insCCTCGTCCTTCT	ENSP00000505508.1:p.Tyr2854_Val2855insLeuValLeuLeu
ENST00000380152.7:c.8561_8562insCCTCGTCCTTCT	ENSP00000369497.3:p.Tyr2854_Val2855insLeuValLeuLeu
ENST00000528762.1:c.59_60insCCTCGTCCTTCT	ENSP00000433168.1:p.Tyr20_Val21insLeuValLeuLeu
ENST00000544455.5:c.8561_8562insCCTCGTCCTTCT	ENSP00000439902.1:p.Tyr2854_Val2855insLeuValLeuLeu
NM_000059.3:c.8561_8562insCCTCGTCCTTCT , LRG_293t1:c.8561_8562insCCTCGTCCTTCT	NP_000050.2:p.Tyr2854_Val2855insLeuValLeuLeu
XM_011535203.1:c.8561_8562insCCTCGTCCTTCT	XP_011533505.1:p.Tyr2854_Val2855insLeuValLeuLeu
XM_011535204.1:c.8465_8466insCCTCGTCCTTCT	XP_011533506.1:p.Tyr2822_Val2823insLeuValLeuLeu
XM_011535205.1:c.8561_8562insCCTCGTCCTTCT	XP_011533507.1:p.Tyr2854_Val2855insLeuValLeuLeu
NM_000059.4:c.8561_8562insCCTCGTCCTTCT MANE Select	NP_000050.3:p.Tyr2854_Val2855insLeuValLeuLeu