Canonical Allele Identifier: CA645585172
Community Standard Title: NM_000059.4(BRCA2):c.5676_5677delinsGG (p.Cys1893Gly)
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32340031_32340032delinsGG , CM000675.2:g.32340031_32340032delinsGG GRCh38
NC_000013.10:g.32914168_32914169delinsGG , CM000675.1:g.32914168_32914169delinsGG GRCh37
NC_000013.9:g.31812168_31812169delinsGG NCBI36
NG_012772.3:g.29552_29553delinsGG , LRG_293:g.29552_29553delinsGG

Transcript Alleles

HGVS Amino-acid Change
NM_000059.4:c.5676_5677delinsGG MANE Select NP_000050.3:p.Cys1893Gly
ENST00000380152.8:c.5676_5677delinsGG MANE Select ENSP00000369497.3:p.Cys1893Gly
NM_000059.3:c.5676_5677delinsGG , LRG_293t1:c.5676_5677delinsGG NP_000050.2:p.Cys1893Gly
ENST00000380152.7:c.5676_5677delinsGG ENSP00000369497.3:p.Cys1893Gly
ENST00000470094.2:c.5676_5677delinsGG ENSP00000434898.2:p.Cys1893Gly
ENST00000528762.2:c.5676_5677delinsGG ENSP00000433168.2:p.Cys1893Gly
ENST00000530893.7:c.5307_5308delinsGG ENSP00000499438.2:p.Cys1770Gly
ENST00000544455.5:c.5676_5677delinsGG ENSP00000439902.1:p.Cys1893Gly
ENST00000544455.6:c.5676_5677delinsGG ENSP00000439902.1:p.Cys1893Gly
ENST00000614259.1:n.5676_5677delinsGG
ENST00000614259.2:c.5676_5677delinsGG ENSP00000506251.1:p.Cys1893Gly
ENST00000665585.2:c.5676_5677delinsGG ENSP00000499570.2:p.Cys1893Gly
ENST00000666593.2:c.5676_5677delinsGG ENSP00000499256.2:p.Cys1893Gly
ENST00000680887.1:c.5676_5677delinsGG ENSP00000505508.1:p.Cys1893Gly
ENST00000700202.2:c.5676_5677delinsGG ENSP00000514856.2:p.Cys1893Gly
XM_011535203.1:c.5676_5677delinsGG XP_011533505.1:p.Cys1893Gly
XM_011535204.1:c.5676_5677delinsGG XP_011533506.1:p.Cys1893Gly
XM_011535205.1:c.5676_5677delinsGG XP_011533507.1:p.Cys1893Gly