Canonical Allele Identifier: CA1087476250

Linked Data

dbSNP Id: rs1799857118

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31654779dup , CM000668.2:g.31654779dup GRCh38
NC_000006.11:g.31622556dup , CM000668.1:g.31622556dup GRCh37
NC_000006.10:g.31730535dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375918.6:c.-102-1693dup (APOM) ENSP00000365083.2:n.-102-1693dup
ENST00000375920.8:c.-102-1693dup (APOM) ENSP00000365085.4:n.-102-1693dup
NM_001256169.1:c.-102-1693dup (APOM) NP_001243098.1:n.-102-1693dup
NR_045828.1:n.143-1693dup (APOM)
XM_011514895.1:c.-13-3003dup (BAG6) XP_011513197.1:n.-13-3003dup
XM_017011279.2:c.-13-3003dup (BAG6) XP_016866768.1:n.-13-3003dup
XM_024446545.1:c.-14+2985dup (BAG6) XP_024302313.1:n.-14+2985dup
NM_001256169.2:c.-102-1693dup (APOM) NP_001243098.1:n.-102-1693dup
NR_045828.2:n.149-1693dup (APOM)