Canonical Allele Identifier: CA2770516633

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31655888del , CM000668.2:g.31655888del GRCh38
NC_000006.11:g.31623665del , CM000668.1:g.31623665del GRCh37
NC_000006.10:g.31731644del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375916.3:c.-79del (APOM) ENSP00000365081.3:n.-79del
ENST00000375918.6:c.-102-584del (APOM) ENSP00000365083.2:n.-102-584del
ENST00000375920.8:c.-102-584del (APOM) ENSP00000365085.4:n.-102-584del
NM_001256169.1:c.-102-584del (APOM) NP_001243098.1:n.-102-584del
NR_045828.1:n.143-584del (APOM)
XM_006715150.2:c.-182del (APOM) XP_006715213.1:n.-182del
XM_011514895.1:c.-13-4112del (BAG6) XP_011513197.1:n.-13-4112del
XM_017011279.2:c.-13-4112del (BAG6) XP_016866768.1:n.-13-4112del
XM_024446545.1:c.-14+1876del (BAG6) XP_024302313.1:n.-14+1876del
NM_001256169.2:c.-102-584del (APOM) NP_001243098.1:n.-102-584del
NR_045828.2:n.149-584del (APOM)