Canonical Allele Identifier: CA1619250641

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657246C= , CM000668.2:g.31657246C= GRCh38
NC_000006.11:g.31625023C= , CM000668.1:g.31625023C= GRCh37
NC_000006.10:g.31733002C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.291C= (APOM) MANE Select ENSP00000365081.3:p.Pro97=
ENST00000375916.3:c.291C= (APOM) ENSP00000365081.3:p.Pro97=
ENST00000375918.6:c.75C= (APOM) ENSP00000365083.2:p.Pro25=
ENST00000375920.8:c.75C= (APOM) ENSP00000365085.4:p.Pro25=
NM_001256169.1:c.75C= (APOM) NP_001243098.1:p.Pro25=
NM_019101.2:c.291C= (APOM) NP_061974.2:p.Pro97=
NR_045828.1:n.326C= (APOM)
XM_006715150.2:c.195C= (APOM) XP_006715213.1:p.Pro65=
XM_011514895.1:c.-14+3075G= (BAG6) XP_011513197.1:p.=
XM_006715150.3:c.195C= (APOM) XP_006715213.1:p.Pro65=
XM_017011279.2:c.-14+3075G= (BAG6) XP_016866768.1:p.=
XM_024446545.1:c.-14+518G= (BAG6) XP_024302313.1:p.=
NM_019101.3:c.291C= (APOM) MANE Select NP_061974.2:p.Pro97=
NM_001256169.2:c.75C= (APOM) NP_001243098.1:p.Pro25=
NR_045828.2:n.332C= (APOM)