Canonical Allele Identifier: CA1619250783

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657573G= , CM000668.2:g.31657573G= GRCh38
NC_000006.11:g.31625350G= , CM000668.1:g.31625350G= GRCh37
NC_000006.10:g.31733329G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.443-52G= (APOM) MANE Select ENSP00000365081.3:n.443-52G=
ENST00000375916.3:c.443-52G= (APOM) ENSP00000365081.3:n.443-52G=
ENST00000375918.6:c.227-52G= (APOM) ENSP00000365083.2:n.227-52G=
ENST00000375920.8:c.227-52G= (APOM) ENSP00000365085.4:n.227-52G=
NM_001256169.1:c.227-52G= (APOM) NP_001243098.1:n.227-52G=
NM_019101.2:c.443-52G= (APOM) NP_061974.2:n.443-52G=
NR_045828.1:n.478-52G= (APOM)
XM_006715150.2:c.347-52G= (APOM) XP_006715213.1:n.347-52G=
XM_011514895.1:c.-14+2748C= (BAG6) XP_011513197.1:n.-14+2748C=
XM_006715150.3:c.347-52G= (APOM) XP_006715213.1:n.347-52G=
XM_017011279.2:c.-14+2748C= (BAG6) XP_016866768.1:n.-14+2748C=
XM_024446545.1:c.-14+191C= (BAG6) XP_024302313.1:n.-14+191C=
NM_019101.3:c.443-52G= (APOM) MANE Select NP_061974.2:n.443-52G=
NM_001256169.2:c.227-52G= (APOM) NP_001243098.1:n.227-52G=
NR_045828.2:n.484-52G= (APOM)