Canonical Allele Identifier: CA2518825385

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31655018del , CM000668.2:g.31655018del GRCh38
NC_000006.11:g.31622795del , CM000668.1:g.31622795del GRCh37
NC_000006.10:g.31730774del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375918.6:c.-102-1454del (APOM) ENSP00000365083.2:n.-102-1454del
ENST00000375920.8:c.-102-1454del (APOM) ENSP00000365085.4:n.-102-1454del
NM_001256169.1:c.-102-1454del (APOM) NP_001243098.1:n.-102-1454del
NR_045828.1:n.143-1454del (APOM)
XM_011514895.1:c.-13-3241del (BAG6) XP_011513197.1:n.-13-3241del
XM_017011279.2:c.-13-3241del (BAG6) XP_016866768.1:n.-13-3241del
XM_024446545.1:c.-14+2747del (BAG6) XP_024302313.1:n.-14+2747del
NM_001256169.2:c.-102-1454del (APOM) NP_001243098.1:n.-102-1454del
NR_045828.2:n.149-1454del (APOM)