Canonical Allele Identifier: CA2677983596

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657187_31657188dup , CM000668.2:g.31657187_31657188dup GRCh38
NC_000006.11:g.31624964_31624965dup , CM000668.1:g.31624964_31624965dup GRCh37
NC_000006.10:g.31732943_31732944dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.270-38_270-37dup (APOM) MANE Select ENSP00000365081.3:n.270-38_270-37dup
ENST00000375916.3:c.270-38_270-37dup (APOM) ENSP00000365081.3:n.270-38_270-37dup
ENST00000375918.6:c.54-38_54-37dup (APOM) ENSP00000365083.2:n.54-38_54-37dup
ENST00000375920.8:c.54-38_54-37dup (APOM) ENSP00000365085.4:n.54-38_54-37dup
NM_001256169.1:c.54-38_54-37dup (APOM) NP_001243098.1:n.54-38_54-37dup
NM_019101.2:c.270-38_270-37dup (APOM) NP_061974.2:n.270-38_270-37dup
NR_045828.1:n.305-38_305-37dup (APOM)
XM_006715150.2:c.174-38_174-37dup (APOM) XP_006715213.1:n.174-38_174-37dup
XM_011514895.1:c.-14+3133_-14+3134dup (BAG6) XP_011513197.1:n.-14+3133_-14+3134dup
XM_006715150.3:c.174-38_174-37dup (APOM) XP_006715213.1:n.174-38_174-37dup
XM_017011279.2:c.-14+3133_-14+3134dup (BAG6) XP_016866768.1:n.-14+3133_-14+3134dup
XM_024446545.1:c.-14+576_-14+577dup (BAG6) XP_024302313.1:n.-14+576_-14+577dup
NM_019101.3:c.270-38_270-37dup (APOM) MANE Select NP_061974.2:n.270-38_270-37dup
NM_001256169.2:c.54-38_54-37dup (APOM) NP_001243098.1:n.54-38_54-37dup
NR_045828.2:n.311-38_311-37dup (APOM)