Canonical Allele Identifier: CA363427668

Gene: APOM BAG6

Linked Data

• MyVariant Identifiers: chr6:g.31625193C>A (hg19) ; chr6:g.31657416C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31657416C>A , CM000668.2:g.31657416C>A	GRCh38
NC_000006.11:g.31625193C>A , CM000668.1:g.31625193C>A	GRCh37
NC_000006.10:g.31733172C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375916.4:c.380C>A (APOM) MANE Select	ENSP00000365081.3:p.Ser127Ter
ENST00000375916.3:c.380C>A (APOM)	ENSP00000365081.3:p.Ser127Ter
ENST00000375918.6:c.164C>A (APOM)	ENSP00000365083.2:p.Ser55Ter
ENST00000375920.8:c.164C>A (APOM)	ENSP00000365085.4:p.Ser55Ter
NM_001256169.1:c.164C>A (APOM)	NP_001243098.1:p.Ser55Ter
NM_019101.2:c.380C>A (APOM)	NP_061974.2:p.Ser127Ter
NR_045828.1:n.415C>A (APOM)
XM_006715150.2:c.284C>A (APOM)	XP_006715213.1:p.Ser95Ter
XM_011514895.1:c.-14+2905G>T (BAG6)	XP_011513197.1:n.-14+2905G>T
XM_006715150.3:c.284C>A (APOM)	XP_006715213.1:p.Ser95Ter
XM_017011279.2:c.-14+2905G>T (BAG6)	XP_016866768.1:n.-14+2905G>T
XM_024446545.1:c.-14+348G>T (BAG6)	XP_024302313.1:n.-14+348G>T
NM_019101.3:c.380C>A (APOM) MANE Select	NP_061974.2:p.Ser127Ter
NM_001256169.2:c.164C>A (APOM)	NP_001243098.1:p.Ser55Ter
NR_045828.2:n.421C>A (APOM)