Canonical Allele Identifier: CA1619250190

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31656162T= , CM000668.2:g.31656162T= GRCh38
NC_000006.11:g.31623939T= , CM000668.1:g.31623939T= GRCh37
NC_000006.10:g.31731918T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.114+82T= (APOM) MANE Select ENSP00000365081.3:n.114+82T=
ENST00000375916.3:c.114+82T= (APOM) ENSP00000365081.3:n.114+82T=
ENST00000375918.6:c.-102-310T= (APOM) ENSP00000365083.2:n.-102-310T=
ENST00000375920.8:c.-102-310T= (APOM) ENSP00000365085.4:n.-102-310T=
NM_001256169.1:c.-102-310T= (APOM) NP_001243098.1:n.-102-310T=
NM_019101.2:c.114+82T= (APOM) NP_061974.2:n.114+82T=
NR_045828.1:n.143-310T= (APOM)
XM_006715150.2:c.11+82T= (APOM) XP_006715213.1:n.11+82T=
XM_011514895.1:c.-14+4159A= (BAG6) XP_011513197.1:n.-14+4159A=
XM_006715150.3:c.11+82T= (APOM) XP_006715213.1:n.11+82T=
XM_017011279.2:c.-14+4159A= (BAG6) XP_016866768.1:n.-14+4159A=
XM_024446545.1:c.-14+1602A= (BAG6) XP_024302313.1:n.-14+1602A=
NM_019101.3:c.114+82T= (APOM) MANE Select NP_061974.2:n.114+82T=
NM_001256169.2:c.-102-310T= (APOM) NP_001243098.1:n.-102-310T=
NR_045828.2:n.149-310T= (APOM)