Canonical Allele Identifier: CA1619250643

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657248G= , CM000668.2:g.31657248G= GRCh38
NC_000006.11:g.31625025G= , CM000668.1:g.31625025G= GRCh37
NC_000006.10:g.31733004G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.293G= (APOM) MANE Select ENSP00000365081.3:p.Arg98=
ENST00000375916.3:c.293G= (APOM) ENSP00000365081.3:p.Arg98=
ENST00000375918.6:c.77G= (APOM) ENSP00000365083.2:p.Arg26=
ENST00000375920.8:c.77G= (APOM) ENSP00000365085.4:p.Arg26=
NM_001256169.1:c.77G= (APOM) NP_001243098.1:p.Arg26=
NM_019101.2:c.293G= (APOM) NP_061974.2:p.Arg98=
NR_045828.1:n.328G= (APOM)
XM_006715150.2:c.197G= (APOM) XP_006715213.1:p.Arg66=
XM_011514895.1:c.-14+3073C= (BAG6) XP_011513197.1:p.=
XM_006715150.3:c.197G= (APOM) XP_006715213.1:p.Arg66=
XM_017011279.2:c.-14+3073C= (BAG6) XP_016866768.1:p.=
XM_024446545.1:c.-14+516C= (BAG6) XP_024302313.1:p.=
NM_019101.3:c.293G= (APOM) MANE Select NP_061974.2:p.Arg98=
NM_001256169.2:c.77G= (APOM) NP_001243098.1:p.Arg26=
NR_045828.2:n.334G= (APOM)