Canonical Allele Identifier: CA2550728202

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31656917C>A , CM000668.2:g.31656917C>A GRCh38
NC_000006.11:g.31624694C>A , CM000668.1:g.31624694C>A GRCh37
NC_000006.10:g.31732673C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375916.4:c.269+291C>A (APOM) MANE Select ENSP00000365081.3:n.269+291C>A
ENST00000375916.3:c.269+291C>A (APOM) ENSP00000365081.3:n.269+291C>A
ENST00000375918.6:c.53+291C>A (APOM) ENSP00000365083.2:n.53+291C>A
ENST00000375920.8:c.53+291C>A (APOM) ENSP00000365085.4:n.53+291C>A
NM_001256169.1:c.53+291C>A (APOM) NP_001243098.1:n.53+291C>A
NM_019101.2:c.269+291C>A (APOM) NP_061974.2:n.269+291C>A
NR_045828.1:n.304+284C>A (APOM)
XM_006715150.2:c.173+284C>A (APOM) XP_006715213.1:n.173+284C>A
XM_011514895.1:c.-14+3404G>T (BAG6) XP_011513197.1:n.-14+3404G>T
XM_006715150.3:c.173+284C>A (APOM) XP_006715213.1:n.173+284C>A
XM_017011279.2:c.-14+3404G>T (BAG6) XP_016866768.1:n.-14+3404G>T
XM_024446545.1:c.-14+847G>T (BAG6) XP_024302313.1:n.-14+847G>T
NM_019101.3:c.269+291C>A (APOM) MANE Select NP_061974.2:n.269+291C>A
NM_001256169.2:c.53+291C>A (APOM) NP_001243098.1:n.53+291C>A
NR_045828.2:n.310+284C>A (APOM)