Canonical Allele Identifier: CA2677982415

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31655860dup , CM000668.2:g.31655860dup GRCh38
NC_000006.11:g.31623637dup , CM000668.1:g.31623637dup GRCh37
NC_000006.10:g.31731616dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375916.3:c.-107dup (APOM) ENSP00000365081.3:n.-107dup
ENST00000375918.6:c.-102-612dup (APOM) ENSP00000365083.2:n.-102-612dup
ENST00000375920.8:c.-102-612dup (APOM) ENSP00000365085.4:n.-102-612dup
NM_001256169.1:c.-102-612dup (APOM) NP_001243098.1:n.-102-612dup
NR_045828.1:n.143-612dup (APOM)
XM_006715150.2:c.-210dup (APOM) XP_006715213.1:n.-210dup
XM_011514895.1:c.-13-4082dup (BAG6) XP_011513197.1:n.-13-4082dup
XM_017011279.2:c.-13-4082dup (BAG6) XP_016866768.1:n.-13-4082dup
XM_024446545.1:c.-14+1906dup (BAG6) XP_024302313.1:n.-14+1906dup
NM_001256169.2:c.-102-612dup (APOM) NP_001243098.1:n.-102-612dup
NR_045828.2:n.149-612dup (APOM)