Canonical Allele Identifier: CA363430584

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657682G>A , CM000668.2:g.31657682G>A GRCh38
NC_000006.11:g.31625459G>A , CM000668.1:g.31625459G>A GRCh37
NC_000006.10:g.31733438G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375916.4:c.500G>A (APOM) MANE Select ENSP00000365081.3:p.Cys167Tyr
ENST00000375916.3:c.500G>A (APOM) ENSP00000365081.3:p.Cys167Tyr
ENST00000375918.6:c.284G>A (APOM) ENSP00000365083.2:p.Cys95Tyr
ENST00000375920.8:c.284G>A (APOM) ENSP00000365085.4:p.Cys95Tyr
NM_001256169.1:c.284G>A (APOM) NP_001243098.1:p.Cys95Tyr
NM_019101.2:c.500G>A (APOM) NP_061974.2:p.Cys167Tyr
NR_045828.1:n.535G>A (APOM)
XM_006715150.2:c.404G>A (APOM) XP_006715213.1:p.Cys135Tyr
XM_011514895.1:c.-14+2639C>T (BAG6) XP_011513197.1:n.-14+2639C>T
XM_006715150.3:c.404G>A (APOM) XP_006715213.1:p.Cys135Tyr
XM_017011279.2:c.-14+2639C>T (BAG6) XP_016866768.1:n.-14+2639C>T
XM_024446545.1:c.-14+82C>T (BAG6) XP_024302313.1:n.-14+82C>T
NM_019101.3:c.500G>A (APOM) MANE Select NP_061974.2:p.Cys167Tyr
NM_001256169.2:c.284G>A (APOM) NP_001243098.1:p.Cys95Tyr
NR_045828.2:n.541G>A (APOM)