Canonical Allele Identifier: CA363427052

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31657256A>T , CM000668.2:g.31657256A>T GRCh38
NC_000006.11:g.31625033A>T , CM000668.1:g.31625033A>T GRCh37
NC_000006.10:g.31733012A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375916.4:c.301A>T (APOM) MANE Select ENSP00000365081.3:p.Ile101Phe
ENST00000375916.3:c.301A>T (APOM) ENSP00000365081.3:p.Ile101Phe
ENST00000375918.6:c.85A>T (APOM) ENSP00000365083.2:p.Ile29Phe
ENST00000375920.8:c.85A>T (APOM) ENSP00000365085.4:p.Ile29Phe
NM_001256169.1:c.85A>T (APOM) NP_001243098.1:p.Ile29Phe
NM_019101.2:c.301A>T (APOM) NP_061974.2:p.Ile101Phe
NR_045828.1:n.336A>T (APOM)
XM_006715150.2:c.205A>T (APOM) XP_006715213.1:p.Ile69Phe
XM_011514895.1:c.-14+3065T>A (BAG6) XP_011513197.1:p.=
XM_006715150.3:c.205A>T (APOM) XP_006715213.1:p.Ile69Phe
XM_017011279.2:c.-14+3065T>A (BAG6) XP_016866768.1:p.=
XM_024446545.1:c.-14+508T>A (BAG6) XP_024302313.1:p.=
NM_019101.3:c.301A>T (APOM) MANE Select NP_061974.2:p.Ile101Phe
NM_001256169.2:c.85A>T (APOM) NP_001243098.1:p.Ile29Phe
NR_045828.2:n.342A>T (APOM)