Canonical Allele Identifier: CA3261215912
Community Standard Title: NM_000059.4(BRCA2):c.8569_8571delinsCCA (p.Ala2857Pro)
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32371037_32371039delinsCCA , CM000675.2:g.32371037_32371039delinsCCA GRCh38
NC_000013.10:g.32945174_32945176delinsCCA , CM000675.1:g.32945174_32945176delinsCCA GRCh37
NC_000013.9:g.31843174_31843176delinsCCA NCBI36
NG_012772.3:g.60558_60560delinsCCA , LRG_293:g.60558_60560delinsCCA

Transcript Alleles

HGVS Amino-acid Change
NM_000059.4:c.8569_8571delinsCCA MANE Select NP_000050.3:p.Ala2857Pro
ENST00000380152.8:c.8569_8571delinsCCA MANE Select ENSP00000369497.3:p.Ala2857Pro
NM_000059.3:c.8569_8571delinsCCA , LRG_293t1:c.8569_8571delinsCCA NP_000050.2:p.Ala2857Pro
ENST00000380152.7:c.8569_8571delinsCCA ENSP00000369497.3:p.Ala2857Pro
ENST00000470094.2:c.8569_8571delinsCCA ENSP00000434898.2:p.Ala2857Pro
ENST00000528762.1:c.67_69delinsCCA ENSP00000433168.1:p.Ala23Pro
ENST00000528762.2:c.8569_8571delinsCCA ENSP00000433168.2:p.Ala2857Pro
ENST00000530893.7:c.8200_8202delinsCCA ENSP00000499438.2:p.Ala2734Pro
ENST00000544455.5:c.8569_8571delinsCCA ENSP00000439902.1:p.Ala2857Pro
ENST00000544455.6:c.8569_8571delinsCCA ENSP00000439902.1:p.Ala2857Pro
ENST00000614259.2:c.8577_8579delinsCCA ENSP00000506251.1:n.8577_8579delinsCCA
ENST00000665585.1:c.1134_1136delinsCCA
ENST00000665585.2:c.8569_8571delinsCCA ENSP00000499570.2:p.Ala2857Pro
ENST00000666593.2:c.8569_8571delinsCCA ENSP00000499256.2:p.Ala2857Pro
ENST00000680887.1:c.8569_8571delinsCCA ENSP00000505508.1:p.Ala2857Pro
ENST00000700202.1:c.1036_1038delinsCCA ENSP00000514856.1:p.Ala346Pro
ENST00000700202.2:c.8569_8571delinsCCA ENSP00000514856.2:p.Ala2857Pro
XM_011535203.1:c.8569_8571delinsCCA XP_011533505.1:p.Ala2857Pro
XM_011535204.1:c.8473_8475delinsCCA XP_011533506.1:p.Ala2825Pro
XM_011535205.1:c.8569_8571delinsCCA XP_011533507.1:p.Ala2857Pro