Canonical Allele Identifier: CA3046517290
Community Standard Title: NM_000059.4(BRCA2):c.2921_2922delinsGA (p.Asp974Gly)
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32337276_32337277delinsGA , CM000675.2:g.32337276_32337277delinsGA GRCh38
NC_000013.10:g.32911413_32911414delinsGA , CM000675.1:g.32911413_32911414delinsGA GRCh37
NC_000013.9:g.31809413_31809414delinsGA NCBI36
NG_012772.3:g.26797_26798delinsGA , LRG_293:g.26797_26798delinsGA

Transcript Alleles

HGVS Amino-acid Change
NM_000059.4:c.2921_2922delinsGA MANE Select NP_000050.3:p.Asp974Gly
ENST00000380152.8:c.2921_2922delinsGA MANE Select ENSP00000369497.3:p.Asp974Gly
NM_000059.3:c.2921_2922delinsGA , LRG_293t1:c.2921_2922delinsGA NP_000050.2:p.Asp974Gly
ENST00000380152.7:c.2921_2922delinsGA ENSP00000369497.3:p.Asp974Gly
ENST00000470094.2:c.2921_2922delinsGA ENSP00000434898.2:p.Asp974Gly
ENST00000528762.2:c.2921_2922delinsGA ENSP00000433168.2:p.Asp974Gly
ENST00000530893.7:c.2552_2553delinsGA ENSP00000499438.2:p.Asp851Gly
ENST00000544455.5:c.2921_2922delinsGA ENSP00000439902.1:p.Asp974Gly
ENST00000544455.6:c.2921_2922delinsGA ENSP00000439902.1:p.Asp974Gly
ENST00000614259.1:n.2921_2922delinsGA
ENST00000614259.2:c.2921_2922delinsGA ENSP00000506251.1:p.Asp974Gly
ENST00000665585.2:c.2921_2922delinsGA ENSP00000499570.2:p.Asp974Gly
ENST00000666593.2:c.2921_2922delinsGA ENSP00000499256.2:p.Asp974Gly
ENST00000680887.1:c.2921_2922delinsGA ENSP00000505508.1:p.Asp974Gly
ENST00000700202.2:c.2921_2922delinsGA ENSP00000514856.2:p.Asp974Gly
XM_011535203.1:c.2921_2922delinsGA XP_011533505.1:p.Asp974Gly
XM_011535204.1:c.2921_2922delinsGA XP_011533506.1:p.Asp974Gly
XM_011535205.1:c.2921_2922delinsGA XP_011533507.1:p.Asp974Gly