Canonical Allele Identifier: CA1087477250

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657156_31657159dup , CM000668.2:g.31657156_31657159dup GRCh38
NC_000006.11:g.31624933_31624936dup , CM000668.1:g.31624933_31624936dup GRCh37
NC_000006.10:g.31732912_31732915dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.270-69_270-66dup (APOM) MANE Select ENSP00000365081.3:n.270-69_270-66dup
ENST00000375916.3:c.270-69_270-66dup (APOM) ENSP00000365081.3:n.270-69_270-66dup
ENST00000375918.6:c.54-69_54-66dup (APOM) ENSP00000365083.2:n.54-69_54-66dup
ENST00000375920.8:c.54-69_54-66dup (APOM) ENSP00000365085.4:n.54-69_54-66dup
NM_001256169.1:c.54-69_54-66dup (APOM) NP_001243098.1:n.54-69_54-66dup
NM_019101.2:c.270-69_270-66dup (APOM) NP_061974.2:n.270-69_270-66dup
NR_045828.1:n.305-69_305-66dup (APOM)
XM_006715150.2:c.174-69_174-66dup (APOM) XP_006715213.1:n.174-69_174-66dup
XM_011514895.1:c.-14+3172_-14+3175dup (BAG6) XP_011513197.1:n.-14+3172_-14+3175dup
XM_006715150.3:c.174-69_174-66dup (APOM) XP_006715213.1:n.174-69_174-66dup
XM_017011279.2:c.-14+3172_-14+3175dup (BAG6) XP_016866768.1:n.-14+3172_-14+3175dup
XM_024446545.1:c.-14+615_-14+618dup (BAG6) XP_024302313.1:n.-14+615_-14+618dup
NM_019101.3:c.270-69_270-66dup (APOM) MANE Select NP_061974.2:n.270-69_270-66dup
NM_001256169.2:c.54-69_54-66dup (APOM) NP_001243098.1:n.54-69_54-66dup
NR_045828.2:n.311-69_311-66dup (APOM)