Canonical Allele Identifier: CA1619250128

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31656007G= , CM000668.2:g.31656007G= GRCh38
NC_000006.11:g.31623784G= , CM000668.1:g.31623784G= GRCh37
NC_000006.10:g.31731763G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.41G= (APOM) MANE Select ENSP00000365081.3:p.Gly14=
ENST00000375916.3:c.41G= (APOM) ENSP00000365081.3:p.Gly14=
ENST00000375918.6:c.-102-465G= (APOM) ENSP00000365083.2:n.-102-465G=
ENST00000375920.8:c.-102-465G= (APOM) ENSP00000365085.4:n.-102-465G=
NM_001256169.1:c.-102-465G= (APOM) NP_001243098.1:n.-102-465G=
NM_019101.2:c.41G= (APOM) NP_061974.2:p.Gly14=
NR_045828.1:n.143-465G= (APOM)
XM_006715150.2:c.-63G= (APOM) XP_006715213.1:n.-63G=
XM_011514895.1:c.-13-4231C= (BAG6) XP_011513197.1:n.-13-4231C=
XM_006715150.3:c.-63G= (APOM) XP_006715213.1:n.-63G=
XM_017011279.2:c.-13-4231C= (BAG6) XP_016866768.1:n.-13-4231C=
XM_024446545.1:c.-14+1757C= (BAG6) XP_024302313.1:n.-14+1757C=
NM_019101.3:c.41G= (APOM) MANE Select NP_061974.2:p.Gly14=
NM_001256169.2:c.-102-465G= (APOM) NP_001243098.1:n.-102-465G=
NR_045828.2:n.149-465G= (APOM)