Canonical Allele Identifier: CA3261215915
Community Standard Title: NM_000059.4(BRCA2):c.8569_8571delinsTCA (p.Ala2857Ser)
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32371037_32371039delinsTCA , CM000675.2:g.32371037_32371039delinsTCA GRCh38
NC_000013.10:g.32945174_32945176delinsTCA , CM000675.1:g.32945174_32945176delinsTCA GRCh37
NC_000013.9:g.31843174_31843176delinsTCA NCBI36
NG_012772.3:g.60558_60560delinsTCA , LRG_293:g.60558_60560delinsTCA

Transcript Alleles

HGVS Amino-acid Change
NM_000059.4:c.8569_8571delinsTCA MANE Select NP_000050.3:p.Ala2857Ser
ENST00000380152.8:c.8569_8571delinsTCA MANE Select ENSP00000369497.3:p.Ala2857Ser
NM_000059.3:c.8569_8571delinsTCA , LRG_293t1:c.8569_8571delinsTCA NP_000050.2:p.Ala2857Ser
ENST00000380152.7:c.8569_8571delinsTCA ENSP00000369497.3:p.Ala2857Ser
ENST00000470094.2:c.8569_8571delinsTCA ENSP00000434898.2:p.Ala2857Ser
ENST00000528762.1:c.67_69delinsTCA ENSP00000433168.1:p.Ala23Ser
ENST00000528762.2:c.8569_8571delinsTCA ENSP00000433168.2:p.Ala2857Ser
ENST00000530893.7:c.8200_8202delinsTCA ENSP00000499438.2:p.Ala2734Ser
ENST00000544455.5:c.8569_8571delinsTCA ENSP00000439902.1:p.Ala2857Ser
ENST00000544455.6:c.8569_8571delinsTCA ENSP00000439902.1:p.Ala2857Ser
ENST00000614259.2:c.8577_8579delinsTCA ENSP00000506251.1:n.8577_8579delinsTCA
ENST00000665585.1:c.1134_1136delinsTCA
ENST00000665585.2:c.8569_8571delinsTCA ENSP00000499570.2:p.Ala2857Ser
ENST00000666593.2:c.8569_8571delinsTCA ENSP00000499256.2:p.Ala2857Ser
ENST00000680887.1:c.8569_8571delinsTCA ENSP00000505508.1:p.Ala2857Ser
ENST00000700202.1:c.1036_1038delinsTCA ENSP00000514856.1:p.Ala346Ser
ENST00000700202.2:c.8569_8571delinsTCA ENSP00000514856.2:p.Ala2857Ser
XM_011535203.1:c.8569_8571delinsTCA XP_011533505.1:p.Ala2857Ser
XM_011535204.1:c.8473_8475delinsTCA XP_011533506.1:p.Ala2825Ser
XM_011535205.1:c.8569_8571delinsTCA XP_011533507.1:p.Ala2857Ser