Canonical Allele Identifier: CA2082822441
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32394734T= , CM000675.2:g.32394734T= GRCh38
NC_000013.10:g.32968871T= , CM000675.1:g.32968871T= GRCh37
NC_000013.9:g.31866871T= NCBI36
NG_012772.3:g.84255T= , LRG_293:g.84255T=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.9302T= ENSP00000434898.2:p.Leu3101=
ENST00000528762.2:c.*669T= ENSP00000433168.2:n.*669T=
ENST00000530893.7:c.8933T= ENSP00000499438.2:p.Leu2978=
ENST00000665585.2:c.*864T= ENSP00000499570.2:n.*864T=
ENST00000666593.2:c.*147T= ENSP00000499256.2:n.*147T=
ENST00000700202.2:c.9251T= ENSP00000514856.2:p.Leu3084=
ENST00000700202.1:c.1718T= ENSP00000514856.1:p.Leu573=
ENST00000700203.1:n.1429T=
ENST00000380152.8:c.9302T= MANE Select ENSP00000369497.3:p.Leu3101=
ENST00000544455.6:c.9302T= ENSP00000439902.1:p.Leu3101=
ENST00000614259.2:c.9310T= ENSP00000506251.1:n.9310T=
ENST00000665585.1:c.2180T=
ENST00000666593.1:c.324T= ENSP00000499256.1:n.324T=
ENST00000680887.1:c.9302T= ENSP00000505508.1:p.Leu3101=
ENST00000380152.7:c.9302T= ENSP00000369497.3:p.Leu3101=
ENST00000470094.1:c.259T=
ENST00000544455.5:c.9302T= ENSP00000439902.1:p.Leu3101=
NM_000059.3:c.9302T= , LRG_293t1:c.9302T= NP_000050.2:p.Leu3101=
XM_011535203.1:c.9302T= XP_011533505.1:p.Leu3101=
XM_011535204.1:c.9206T= XP_011533506.1:p.Leu3069=
NM_000059.4:c.9302T= MANE Select NP_000050.3:p.Leu3101=