Canonical Allele Identifier: CA1619250778

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657566A= , CM000668.2:g.31657566A= GRCh38
NC_000006.11:g.31625343A= , CM000668.1:g.31625343A= GRCh37
NC_000006.10:g.31733322A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.443-59A= (APOM) MANE Select ENSP00000365081.3:n.443-59A=
ENST00000375916.3:c.443-59A= (APOM) ENSP00000365081.3:n.443-59A=
ENST00000375918.6:c.227-59A= (APOM) ENSP00000365083.2:n.227-59A=
ENST00000375920.8:c.227-59A= (APOM) ENSP00000365085.4:n.227-59A=
NM_001256169.1:c.227-59A= (APOM) NP_001243098.1:n.227-59A=
NM_019101.2:c.443-59A= (APOM) NP_061974.2:n.443-59A=
NR_045828.1:n.478-59A= (APOM)
XM_006715150.2:c.347-59A= (APOM) XP_006715213.1:n.347-59A=
XM_011514895.1:c.-14+2755T= (BAG6) XP_011513197.1:n.-14+2755T=
XM_006715150.3:c.347-59A= (APOM) XP_006715213.1:n.347-59A=
XM_017011279.2:c.-14+2755T= (BAG6) XP_016866768.1:n.-14+2755T=
XM_024446545.1:c.-14+198T= (BAG6) XP_024302313.1:n.-14+198T=
NM_019101.3:c.443-59A= (APOM) MANE Select NP_061974.2:n.443-59A=
NM_001256169.2:c.227-59A= (APOM) NP_001243098.1:n.227-59A=
NR_045828.2:n.484-59A= (APOM)