Canonical Allele Identifier: CA1619250188

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31656155G= , CM000668.2:g.31656155G= GRCh38
NC_000006.11:g.31623932G= , CM000668.1:g.31623932G= GRCh37
NC_000006.10:g.31731911G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.114+75G= (APOM) MANE Select ENSP00000365081.3:n.114+75G=
ENST00000375916.3:c.114+75G= (APOM) ENSP00000365081.3:n.114+75G=
ENST00000375918.6:c.-102-317G= (APOM) ENSP00000365083.2:n.-102-317G=
ENST00000375920.8:c.-102-317G= (APOM) ENSP00000365085.4:n.-102-317G=
NM_001256169.1:c.-102-317G= (APOM) NP_001243098.1:n.-102-317G=
NM_019101.2:c.114+75G= (APOM) NP_061974.2:n.114+75G=
NR_045828.1:n.143-317G= (APOM)
XM_006715150.2:c.11+75G= (APOM) XP_006715213.1:n.11+75G=
XM_011514895.1:c.-14+4166C= (BAG6) XP_011513197.1:n.-14+4166C=
XM_006715150.3:c.11+75G= (APOM) XP_006715213.1:n.11+75G=
XM_017011279.2:c.-14+4166C= (BAG6) XP_016866768.1:n.-14+4166C=
XM_024446545.1:c.-14+1609C= (BAG6) XP_024302313.1:n.-14+1609C=
NM_019101.3:c.114+75G= (APOM) MANE Select NP_061974.2:n.114+75G=
NM_001256169.2:c.-102-317G= (APOM) NP_001243098.1:n.-102-317G=
NR_045828.2:n.149-317G= (APOM)