Canonical Allele Identifier: CA1619250680

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657355A= , CM000668.2:g.31657355A= GRCh38
NC_000006.11:g.31625132A= , CM000668.1:g.31625132A= GRCh37
NC_000006.10:g.31733111A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375916.4:c.344-25A= (APOM) MANE Select ENSP00000365081.3:n.344-25A=
ENST00000375916.3:c.344-25A= (APOM) ENSP00000365081.3:n.344-25A=
ENST00000375918.6:c.128-25A= (APOM) ENSP00000365083.2:n.128-25A=
ENST00000375920.8:c.128-25A= (APOM) ENSP00000365085.4:n.128-25A=
NM_001256169.1:c.128-25A= (APOM) NP_001243098.1:n.128-25A=
NM_019101.2:c.344-25A= (APOM) NP_061974.2:n.344-25A=
NR_045828.1:n.379-25A= (APOM)
XM_006715150.2:c.248-25A= (APOM) XP_006715213.1:n.248-25A=
XM_011514895.1:c.-14+2966T= (BAG6) XP_011513197.1:n.-14+2966T=
XM_006715150.3:c.248-25A= (APOM) XP_006715213.1:n.248-25A=
XM_017011279.2:c.-14+2966T= (BAG6) XP_016866768.1:n.-14+2966T=
XM_024446545.1:c.-14+409T= (BAG6) XP_024302313.1:n.-14+409T=
NM_019101.3:c.344-25A= (APOM) MANE Select NP_061974.2:n.344-25A=
NM_001256169.2:c.128-25A= (APOM) NP_001243098.1:n.128-25A=
NR_045828.2:n.385-25A= (APOM)